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S.P. Singh solutions for कन्साइस केमिस्ट्री [इंग्रजी] इयत्ता १० आयसीएसई0 chapter 12 - Organic Chemistry [Latest edition]

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S.P. Singh solutions for कन्साइस केमिस्ट्री [इंग्रजी] इयत्ता १० आयसीएसई0 chapter 12 - Organic Chemistry - Shaalaa.com
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Solutions for Chapter 12: Organic Chemistry

Below listed, you can find solutions for Chapter 12 of CISCE S.P. Singh for कन्साइस केमिस्ट्री [इंग्रजी] इयत्ता १० आयसीएसई0.


Intext QuestionsIntext QuestionsEXERCISE-12AEXERCISE-12BEXERCISE-12CEXERCISE-12DEXERCISE-12EEXERCISE-12FMISCELLANEOUS
Intext Questions [Page 187]

S.P. Singh solutions for कन्साइस केमिस्ट्री [इंग्रजी] इयत्ता १० आयसीएसई0 12 Organic Chemistry Intext Questions [Page 187]

Intext Questions | Q 1. (a) | Page 187

What are organic compounds?

Intext Questions | Q 1. (b) (i) | Page 187

What is vital force theory?

Intext Questions | Q 1. (b) (ii) | Page 187

Why vital force theory was discarded?

Intext Questions | Q 2. (a) | Page 187

Name a few sources of organic chemistry?

Intext Questions | Q 2. (b) | Page 187

Give the various applications of organic chemistry?

Intext Questions | Q 3. | Page 187

Organic chemistry plays a key role in all walks of life. Discuss.

Intext Questions | Q 4. | Page 187

Carbon shows some unique properties; name them.

Intext Questions | Q 5. (a) | Page 187

Explain the following:

Tetravalency

Intext Questions | Q 5. (b) | Page 187

Explain the following:

Catenation 

Intext Questions | Q 6. | Page 187

Write any four properties of organic compounds that distinguish them from inorganic compounds.

Intext Questions | Q 7. | Page 187

Why are organic compounds studies as a separate branch of chemistry?

Intext Questions | Q 8. (i) | Page 187

What are hydrocarbons?

Intext Questions | Q 8. (ii) | Page 187

Compare saturated and unsaturated hydrocarbons.

Intext Questions | Q 9. | Page 187

Give reasons for the existence of the large number of organic compounds.

Intext Questions | Q 10. (a) | Page 187

Give at least one example to show the structure of isomers of single-bond compound.

Intext Questions | Q 10. (b) | Page 187

Give at least one example to show the structure of isomers of double bond compounds.

Intext Questions | Q 10. (c) | Page 187

Give at least one example in case to show the structure of isomers of a triple bond compound.

Intext Questions | Q 11. (a) | Page 187

Name a compound and draw the figure:

Cyclic compound with a single bond.

Intext Questions | Q 11. (b) | Page 187

Name a compound and draw the figure:

Cyclic compound with the triple bond.

Intext Questions | Q 12. (a) | Page 187

Give the name of one member of the saturated hydrocarbons.

Intext Questions | Q 12. (b) | Page 187

Give the name of one member of the unsaturated hydrocarbons.

Intext Questions | Q 13. (i) | Page 187

Define the substitution reaction. Give an example.

Intext Questions | Q 13. (ii) | Page 187

Define the addition reaction. Give an example.

Intext Questions [Page 190]

S.P. Singh solutions for कन्साइस केमिस्ट्री [इंग्रजी] इयत्ता १० आयसीएसई0 12 Organic Chemistry Intext Questions [Page 190]

Intext Questions | Q 1. (i) | Page 190

Define a functional group.

Intext Questions | Q 1. (ii) (a) | Page 190

Give the structural formula of the following functional group:

Ketone

Intext Questions | Q 1. (ii) (b) | Page 190

Give the structural formula of the following functional group:

Alcohols

Intext Questions | Q 1. (ii) (c) | Page 190

Give the structural formula of the following functional group:

Aldehydes

Intext Questions | Q 2. (a) | Page 190

What is a homologous series?

Intext Questions | Q 2. (b) (i) | Page 190

What is the difference in the molecular formula of any two adjacent homologues in terms of molecular mass?

Intext Questions | Q 2. (b) (ii) | Page 190
What is the difference in the molecular formula of any two adjacent homologues in terms of the number and kind of atoms per molecule?
Intext Questions | Q 3. (a) | Page 190

Write the name and formula of the fourth member of the following homologous series:

Alkyne

Intext Questions | Q 3. (b) | Page 190

Write the name and formula of the fourth member of the following homologous series:

Alcohol

Intext Questions | Q 4. (i) | Page 190

Which part of an organic compound determines physical properties?

Intext Questions | Q 4. (ii) | Page 190

Which part of an organic compound determines chemical properties?

Intext Questions | Q 5. (a) | Page 190

Name the alkyl radical and the functional group of the following organic compound:

CH3OH

Intext Questions | Q 5. (b) | Page 190

Name the alkyl radical and the functional group of the following organic compound:

C2H5OH

Intext Questions | Q 5. (c) | Page 190

Name the alkyl radical and the functional group of the following organic compound:

C3H7CHO

Intext Questions | Q 5. (d) | Page 190

Name the alkyl radical and the functional group of the following organic compound:

C4H9COOH

Intext Questions | Q 5. (e) | Page 190

Name the alkyl radical and the functional group of the following organic compound:

CH3COOH

Intext Questions | Q 5. (f) | Page 190

Name the alkyl radical and the functional group of the following organic compound:

HCHO

Intext Questions | Q 6. (a) | Page 190

What is an alkyl group?

Intext Questions | Q 6. (b) | Page 190

Give the names of any three alkyl groups. How are they formed?

Intext Questions | Q 7. | Page 190

Give the names and the structural formula of the first three members of the homologous series of alkanes.

EXERCISE-12A [Pages 196 - 198]

S.P. Singh solutions for कन्साइस केमिस्ट्री [इंग्रजी] इयत्ता १० आयसीएसई0 12 Organic Chemistry EXERCISE-12A [Pages 196 - 198]

EXERCISE-12A | Q 1. (a) | Page 196

Write the IUPAC name of the following:

\[\begin{array}{cc}
\phantom{...}\ce{CH3}\\
|\\
\ce{CH3 - C - CH3}\\
|\\
\phantom{...}\ce{CH3}
\end{array}\]

EXERCISE-12A | Q 1. (b) | Page 196

Write the IUPAC name of the following:

\[\begin{array}{cc}
\ce{CH3 - CH - CH2 - CH3}\\
|\phantom{.........}\\
\ce{CH3}\phantom{......}
\end{array}\]

EXERCISE-12A | Q 1. (c) | Page 196

Write the IUPAC name of the following:

\[\begin{array}{cc}
\phantom{.}\ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H}\\
\phantom{.}|\phantom{....}|\phantom{....}|\phantom{}\\
\ce{H - C = C - C - H}\\
\phantom{.........}|\\
\phantom{.........}\ce{H}
\end{array}\]

EXERCISE-12A | Q 1. (d) | Page 196

Write the IUPAC name of the following:

\[\begin{array}{cc}
\ce{CH3}\phantom{......}\\
|\phantom{.........}\\
\ce{H3C - C - CH2CH2CH3}\\
|\phantom{.........}\\
\ce{CH3}\phantom{.......}
\end{array}\]

EXERCISE-12A | Q 1. (e) | Page 196

Write the IUPAC name of the following:

CH3 – C ≡ C – CH2CH3

EXERCISE-12A | Q 1. (f) | Page 196

Write the IUPAC name of the following:

\[\begin{array}{cc}
\phantom{............}\ce{CH3}\\
\phantom{.........}|\\
\ce{H - C ≡ C - C - H}\\
\phantom{.........}|\\
\phantom{............}\ce{CH3}
\end{array}\]

EXERCISE-12A | Q 1. (g) | Page 196

Write the IUPAC name of the following:

\[\begin{array}{cc}
\ce{Cl}\phantom{...........}\\
|\phantom{............}\\
\ce{CH3 - CH - CH - CH2CH3}\\
|\\
\phantom{.}\ce{Cl}
\end{array}\]

EXERCISE-12A | Q 1. (h) | Page 196

Write the IUPAC name of the following:

\[\begin{array}{cc}
\ce{CH3}\phantom{...}\ce{CH3}\phantom{......}\\
|\phantom{......}|\phantom{.........}\\
\ce{CH2 - CH - CH2}\\
\phantom{...........}|\\
\phantom{.....................}\ce{CH2CH2CH3}
\end{array}\]

EXERCISE-12A | Q 1. (i) | Page 196

Write the IUPAC name of the following:

\[\begin{array}{cc}
\ce{H}\phantom{...}\ce{H}\\
|\phantom{....}|\\
\ce{H3C - C = C - CH3}\\
\end{array}\]

EXERCISE-12A | Q 1. (j) | Page 196

Write the IUPAC name of the following:

CH3 – C ≡ C – CH2CH2CH2CH3

EXERCISE-12A | Q 1. (k) | Page 196

Write the IUPAC name of the following:

\[\begin{array}{cc}
\ce{CH3}\phantom{...........}\\
|\phantom{.............}\\
\ce{CH3 - C - CH2CH2CH2CHO}\\
|\phantom{.............}\\
\ce{CH3}\phantom{...........}\\
\end{array}\]

EXERCISE-12A | Q 1. (l) | Page 196

Write the IUPAC name of the following:

\[\begin{array}{cc}
\ce{CH3 - CH - CH2CH2CH3}\\
|\phantom{..........}\\
\ce{OH}\phantom{........}\\
\end{array}\]

EXERCISE-12A | Q 1. (m) | Page 196

Write the IUPAC name of the following:

\[\begin{array}{cc}
\ce{CH3CHCH2CH2COOH}\\
|\phantom{.............}\\
\ce{CH3}\phantom{...........}\\
\end{array}\]

EXERCISE-12A | Q 1. (n) | Page 196

Write the IUPAC name of the following:

\[\begin{array}{cc}
\ce{CH3}\phantom{.}\\
|\phantom{....}\\
\ce{CH3 - C - CH2CH3}\\
|\phantom{....}\\
\ce{Br}\phantom{...}\\
\end{array}\]

EXERCISE-12A | Q 1. (o) | Page 196

Write the IUPAC name of the following:

\[\begin{array}{cc}
\ce{CH3}\phantom{........}\\
|\phantom{...........}\\
\ce{CH3 - CH - CH2 - CH2Br}
\end{array}\]

EXERCISE-12A | Q 1. (p) | Page 196

Write the IUPAC name of the following:

\[\begin{array}{cc}
\ce{H}\phantom{.........}\\
|\phantom{.........}\\
\ce{H - C - C ≡ C - H}\\
|\phantom{.........}\\
\ce{H}\phantom{.........}
\end{array}\]

EXERCISE-12A | Q 1. (q) | Page 196

Write the IUPAC name of the following:

\[\begin{array}{cc}
\ce{H - C = O}\\
|\\
\ce{H}
\end{array}\]

EXERCISE-12A | Q 1. (r) | Page 196

Write the IUPAC name of the following:

\[\begin{array}{cc}
\ce{H}\phantom{.........}\\
|\phantom{.........}\\
\ce{H - C - C ≡ C - H}\\
|\phantom{.........}\\
\ce{H}\phantom{.........}
\end{array}\]

EXERCISE-12A | Q 1. (s) | Page 196

Give the IUPAC name of the following:

\[\begin{array}{cc}
\phantom{}\ce{H}\phantom{...}\ce{H}\phantom{...}\ce{H}\phantom{..}\\
\phantom{}|\phantom{....}|\phantom{....}|\phantom{..}\\
\ce{H - C - C - C - OH}\\
\phantom{}|\phantom{....}|\phantom{....}|\phantom{..}\\
\ce{\phantom{}H\phantom{...}H\phantom{...}H\phantom{..}}
\end{array}\]

EXERCISE-12A | Q 1. (t) | Page 196

Write the IUPAC name of the following:

\[\begin{array}{cc}
\ce{\phantom{.....}H\phantom{...}O}\\
\phantom{.....}|\phantom{....}||\\
\ce{H - C - C}\\
\phantom{.....}|\phantom{....}|\\
\ce{\phantom{.......}H\phantom{...}OH}\\
\end{array}\]

EXERCISE-12A | Q 1. (u) | Page 197

Write the IUPAC name of the following:

\[\begin{array}{cc}
\ce{H\phantom{...}O}\\
|\phantom{....}||\\
\ce{H - C - C - H}\\
|\phantom{.....}\\
\ce{H}\phantom{.....}
\end{array}\]

EXERCISE-12A | Q 1. (v) | Page 197

Write the IUPAC name of the following:

\[\begin{array}{cc}
\ce{H\phantom{...}H}\\
|\phantom{....}|\\
\ce{H - C - C - H}\\
|\phantom{....}|\\
\ce{Cl\phantom{...}Cl}\\\end{array}\]

EXERCISE-12A | Q 2. (a) | Page 197

Write the structure of the following compound:

Prop-1-ene

EXERCISE-12A | Q 2. (b) | Page 197

Draw the structural formula for the following:

2, 3-dimethyl butane

EXERCISE-12A | Q 2. (c) | Page 197

Give the structural formulae of the following:

2-methyl propane

EXERCISE-12A | Q 2. (d) | Page 197

Write the structure of the following compound:

3-hexene

EXERCISE-12A | Q 2. (e) | Page 197

Write the structure of the following compound:

prop-1-yne

EXERCISE-12A | Q 2. (f) | Page 197

Write the structure of the following compound:

2-methylprop-1-ene

EXERCISE-12A | Q 2. (g) | Page 197

Write the structure of the following compound:

Alcohol with the molecular formula C4H10O.

Choose the correct answer:

EXERCISE-12A | Q 3. (a) | Page 197

C5H11 is an ______.

  • alkane

  • alkene

  • alkyne

  • alkyl group

EXERCISE-12A | Q 3. (b) | Page 197

A hydrocarbon of the general formula CnH2n is ______.

  • C15H30

  • C12H26

  • C8H20

  • C6H14

EXERCISE-12A | Q 3. (c) | Page 197

The total number of different carbon chains that four carbon atoms form in alkane is ______.

  • 5

  • 4

  • 3

  • 2

EXERCISE-12A | Q 3. (d) | Page 197

CH3 – CH2 – OH and CH3 – O – CH3 are ______.

  • position isomers

  • chain isomers

  • homologous

  • functional group isomers

EXERCISE-12A | Q 3. (e) | Page 197

The IUPAC name of the compound is

\[\begin{array}{cc}
\phantom{........}\ce{CH3}\\
\phantom{......}|\\
\ce{CH3 - CH2 - CH2 - CH - CH2 - CH3}
\end{array}\]

  • 3-trimethylhexane

  • 3-methylhexane

  • 4-methylhexane

Fill in the blanks.

EXERCISE-12A | Q 4. (a) | Page 197

Propane and ethane are ______.

  • homologues

  • isomers

EXERCISE-12A | Q 4. (b) | Page 197

A saturated hydrocarbon does not participate in a/an ______ reaction.

  • substitution

  • addition

EXERCISE-12A | Q 4. (c) | Page 197

Succeeding members of a homologous series differ by ______.

  • CH

  • CH2

  • CH3

EXERCISE-12A | Q 4. (d) | Page 197

As the molecular masses of hydrocarbons increase, their boiling points ______ and melting points ______.

  • increase

  • decrease

EXERCISE-12A | Q 4. (e) | Page 197

C25H52 and C50H102 belong to ______ homologous series.

  • the same

  • different

EXERCISE-12A | Q 4. (f) | Page 197

CO is an ______ compound.

  • organic

  • inorganic

EXERCISE-12A | Q 4. (g) | Page 197

The chemical properties of an organic compound are largely decided by the ______ and the physical properties of an organic compound are largely decided by the ______.

  • functional group

  • number of carbon atoms

EXERCISE-12A | Q 4. (h) | Page 197

CHO is the functional group of an ______.

  • alcohol

  • aldehyde

EXERCISE-12A | Q 4. (i) | Page 197

The root word in the IUPAC name of an organic compound depends upon the number of carbon atoms in ______.

  • any chain

  • principal chain

EXERCISE-12A | Q 4. (j) | Page 197

But-1-ene and but-2-ene are examples of ______ isomerism.

  • chain

  • position

  • functional

EXERCISE-12A | Q 5. i. a. | Page 197

Define of chain isomerism.

EXERCISE-12A | Q 5. i. b. | Page 197

Explain of chain isomerism with an example.

EXERCISE-12A | Q 5. ii. | Page 197

Define or explain position isomerism with an example.

EXERCISE-12A | Q 6. (a) i. | Page 197

Define isomerism.

EXERCISE-12A | Q 6. (a) ii. | Page 197

State two main causes of isomerism.

EXERCISE-12A | Q 6. (b) | Page 197

Draw the chain isomers of hexane (C6H14).

EXERCISE-12A | Q 6. (c) | Page 197

Draw position isomers of butene (C4H8).

EXERCISE-12A | Q 7. (a) | Page 197

Draw the structural formula for the isomer of the n-butane compound. What compound is used to describe this compound taken together?

EXERCISE-12A | Q 7. (b) | Page 197

Draw the structural formula for the vinegar compound. What compound is used to describe this compound taken together?

EXERCISE-12A | Q 7. (c) | Page 197

Draw the structural formula for the 2-propanol compound. What compound is used to describe this compound taken together?

EXERCISE-12A | Q 7. (d) | Page 197

Draw the structural formula for the ethanal compound. What compound is used to describe this compound taken together?

EXERCISE-12A | Q 7. (e) | Page 197

Draw the structural formula for the acetone compound. What compound is used to describe this compound taken together?

EXERCISE-12A | Q 7. (f) | Page 197

Draw the structural formula for the diethyl ether compound. What compound is used to describe this compound taken together?

EXERCISE-12A | Q 8. (a) (i) | Page 197

What is the special feature of the structure of ethene?

EXERCISE-12A | Q 8. (a) (ii) | Page 197

What is the special feature of the structure of ethyne?

EXERCISE-12A | Q 8. (b) | Page 197

What type of reaction is common to both the ethene and ethyne compounds? Why methane does not undergo this type of reaction?

EXERCISE-12A | Q 8. (c) | Page 197

What is the IUPAC name of dimethyl ether?

EXERCISE-12A | Q 9. (i) | Page 197

Which type of reaction will ethane undergo?

EXERCISE-12A | Q 9. (ii) | Page 197

Which type of reaction will ethene undergo?

EXERCISE-12A | Q 10. | Page 197

Choosing only words from the following list, write down appropriate words to fill in the blanks from (a) to (e) given below.

[Addition, carbohydrates, CnH2n−2, CnH2n, CnH2n+2, electrochemical homologous, hydrocarbon, saturated, substitution, unsaturated]

The alkanes from an (a) ______ series with the general formula (b) ______. The alkanes are (c) ______ (d) ______ which generally undergo (e) ______ reactions.

EXERCISE-12A | Q 11. (a) | Page 197

Draw the structural formula of a compound with two carbon atoms in the following case:

An alkane with a carbon to carbon single bond.

EXERCISE-12A | Q 11. (b) | Page 197

Draw the structural formula of a compound with two carbon atoms in the following case:

An alcohol containing two carbon atoms.

EXERCISE-12A | Q 11. (c) | Page 197

Draw the structural formula of a compound with two carbon atoms in the following case:

An unsaturated hydrocarbon with carbon to carbon triple bond.

EXERCISE-12A | Q 12. (a) | Page 197

From the given list, name the compound with −OH as part of its structure.

  • Ethane

  • Ethene

  • Ethanoic acid

  • Ethyne

  • Ethanol

EXERCISE-12A | Q 12. (b) | Page 197

From the given list, name the compound with –COOH as part of its structure.

  • Ethane

  • Ethene

  • Ethanoic acid

  • Ethyne

  • Ethanol

EXERCISE-12A | Q 12. (c) | Page 197

From the given list, name the homologue of the homologous series with the general formula CnH2n.

  • Ethane

  • Ethene

  • Ethanoic acid

  • Ethyne

  • Ethanol

EXERCISE-12A | Q 13. (a) | Page 197

Give the correct IUPAC name and the functional group for the compound whose structural formula is given below:

\[\begin{array}{cc}
\ce{H}\phantom{...}\ce{H}\phantom{...}\ce{O}\\
\phantom{.}|\phantom{....}|\phantom{....}||\\
\ce{H - C - C - C - H}\\
|\phantom{....}|\phantom{.....}\\
\ce{H}\phantom{...}\ce{H}\phantom{.....}\\
\end{array}\]

EXERCISE-12A | Q 13. (b) | Page 197

Give the correct IUPAC name and the functional group for the compound whose structural formula is given below:

\[\begin{array}{cc}
\ce{H\phantom{...}H\phantom{...}H\phantom{..}}\\
|\phantom{....}|\phantom{....}|\phantom{..}\\
\ce{H - C - C - C - OH}\\
|\phantom{....}|\phantom{....}|\phantom{..}\\
\ce{H\phantom{...}H\phantom{...}H\phantom{..}}
\end{array}\]

EXERCISE-12A | Q 14. | Page 198

Copy and complete the following table, which relates to the three homologous series of hydrocarbons:

General formula CnH2n CnH2n-2 CnH2n+2
IUPAC name of the homologus series      
Characteristic bond type     Single bonds
IUPAC name of the first member of the series      
Type of reaction with chlorine   Addition  
EXERCISE-12A | Q 15. (a) | Page 198

Fill in the blanks with the correct words from the brackets:

Alkenes are the (i) ______ (analogous/homologous) series of (ii) ______ (saturated/unsaturated) hydrocarbons. They differ from alkanes due to the presence of (iii) ______ (double/single) bonds. Alkenes mainly undergo (iv) ______ (addition/substitution) reactions.

EXERCISE-12A | Q 15. (b) | Page 198

The organic compound which undergoes substitution reaction is ______.

  • C2H2

  • C2H4

  • C10H18

  • C2H6

EXERCISE-12A | Q 15. (c) | Page 198

Draw the structural formulae of the two isomers of Butane. Give the correct IUPAC name of each of the isomers.

EXERCISE-12A | Q 16. (a) | Page 198

Name the saturated hydrocarbon containing two carbon atoms.

EXERCISE-12A | Q 16. (b) | Page 198

Name an alcohol with three carbon atoms.

EXERCISE-12A | Q 16. (c) | Page 198

Name a triple bond hydrocarbon with two carbon atoms.

EXERCISE-12B [Page 203]

S.P. Singh solutions for कन्साइस केमिस्ट्री [इंग्रजी] इयत्ता १० आयसीएसई0 12 Organic Chemistry EXERCISE-12B [Page 203]

EXERCISE-12B | Q 1. | Page 203

State the sources of Alkanes.

EXERCISE-12B | Q 2. | Page 203

Methane is a greenhouse gas. comment.

EXERCISE-12B | Q 3. | Page 203

Give the general formula of alkanes. 

EXERCISE-12B | Q 4. (a) | Page 203

Draw the structures of isomers of butane. Write the IUPAC and common names of these isomers.

EXERCISE-12B | Q 4. (b) | Page 203

Draw the structures of the isomer of pentane. Write the IUPAC and common names of these isomer

EXERCISE-12B | Q 5. (a) i. | Page 203

Write the molecular formula of methane.

EXERCISE-12B | Q 5. (a) ii. | Page 203

Write the molecular formula of ethane.

EXERCISE-12B | Q 5. (b) i. | Page 203

Write the electron dot formula of methane.

EXERCISE-12B | Q 5. (b) ii. | Page 203

Write the electron dot formula of ethane.

EXERCISE-12B | Q 5. (c) i. | Page 203

Write the structural formula of methane.

EXERCISE-12B | Q 5. (c) ii. | Page 203

Write the structural formulae of the following compound:

Ethane

EXERCISE-12B | Q 6. (a) | Page 203

How is methane prepared in the laboratory?

EXERCISE-12B | Q 6. (b) | Page 203

How is ethane prepared in the laboratory?

EXERCISE-12B | Q 7. i. | Page 203

How is methane prepared from methyl iodide?

EXERCISE-12B | Q 7. ii | Page 203

How is ethane prepared from ethyl bromide?

EXERCISE-12B | Q 8. i. | Page 203

What is the substitution reaction?

EXERCISE-12B | Q 8. ii. | Page 203

Give the reaction of chlorine with ethane and name the product formed. 

EXERCISE-12B | Q 9. (a) | Page 203

Name the compounds formed when methane burns in sufficient air. Give a balanced equation.

EXERCISE-12B | Q 9. (b) | Page 203

Name the compounds formed when methane burns in insufficient air. Give a balanced equation.

EXERCISE-12B | Q 10. (a) (i) | Page 203

Write the names and formulas of the products formed when methane reacts with chlorine. Write the chemical equations.

EXERCISE-12B | Q 10. (a) (ii) | Page 203

Write the names and the formula of the products formed when methane reacts with bromine. Write the chemical equations.

EXERCISE-12B | Q 10. (b) (i) | Page 203

Write the names and the formula of the products formed when ethane reacts with chlorine. Write the chemical equations.

EXERCISE-12B | Q 10. (b) (ii) | Page 203

Write the names and the formula of the products formed when ethane reacts with bromine. Write the chemical equations.

EXERCISE-12B | Q 11. (a) | Page 203

Name the compound prepared from sodium propionate. Write the balanced equation for the same.

EXERCISE-12B | Q 11. (b) | Page 203

Name the compound prepared from methyl iodide. Write the balanced equation for the same.

EXERCISE-12B | Q 11. (c) | Page 203

Name the compound prepared from ethyl bromide. Write a balanced equation for the same.

EXERCISE-12B | Q 12. (i) | Page 203

Write the equation for the complete combustion of methane.

EXERCISE-12B | Q 12. (ii) | Page 203

Write the balanced equation for the complete combustion of ethane.

EXERCISE-12B | Q 13. (a) | Page 203

Convert methane into chloroform.

EXERCISE-12B | Q 13. (b) | Page 203

Convert sodium acetate into methane.

EXERCISE-12B | Q 13. (c) | Page 203

Convert methyl iodide into ethane.

EXERCISE-12B | Q 13. (d) | Page 203

Convert methane to methyl alcohol.

EXERCISE-12B | Q 14. (a) | Page 203

Give three uses of methane.

EXERCISE-12B | Q 14. (b) | Page 203

Give three uses of ethane.

EXERCISE-12B | Q 15. (a) | Page 203

Under what conditions does ethane get converted to ethyl alcohol?

EXERCISE-12B | Q 15. (b) | Page 203

Under what conditions does ethane get converted to acetaldehyde?

EXERCISE-12B | Q 15. (c) | Page 203

Under what conditions does ethane get converted to acetic acid?

EXERCISE-12B | Q 16. i. | Page 203

Using appropriate catalysts, ethane can be oxidized to an alcohol. Name the alcohol formed when ethane is oxidized.

EXERCISE-12B | Q 16. ii. | Page 203

Using appropriate catalysts, ethane can be oxidized to an aldehyde. Name the aldehyde formed when ethane is oxidized.

EXERCISE-12B | Q 16. iii. | Page 203

Using appropriate catalysts, ethane can be oxidized to an acid. Name the acid formed when ethane is oxidized.

EXERCISE-12C [Page 207]

S.P. Singh solutions for कन्साइस केमिस्ट्री [इंग्रजी] इयत्ता १० आयसीएसई0 12 Organic Chemistry EXERCISE-12C [Page 207]

EXERCISE-12C | Q 1. (a) | Page 207

Write the molecular formula of ethene (Ethylene).

EXERCISE-12C | Q 1. (b) | Page 207

Write the electron dot formula of ethene (ethylene).

EXERCISE-12C | Q 1. (c) | Page 207

Write the structural formula of ethene (ethylene).

EXERCISE-12C | Q 2. (a) i. | Page 207

The molecules of the alkene family are represented by a general formula CnH2n. Answer the following:

What does n signify?

EXERCISE-12C | Q 2. (a) ii. | Page 207

The molecules of the alkene family are represented by a general formula CnH2n. Answer the following:

What does 2n signify?

EXERCISE-12C | Q 2. (b) | Page 207

The molecules of the alkene family are represented by a general formula CnH2n. Answer the following:

What is the name of the alkene when n = 4? 

EXERCISE-12C | Q 2. (c) | Page 207

The molecules of the alkene family are represented by a general formula, CnH2n. Answer the following:

What is the molecular formula of alkene when n = 4? 

EXERCISE-12C | Q 2. (d) | Page 207

The molecules of the alkene family are represented by a general formula CnH2n. Answer the following:

What is the molecular formula of the alkene if there are ten H atoms in it? 

EXERCISE-12C | Q 2. (e) | Page 207

The molecules of the alkene family are represented by a general formula CnH2n. Answer the following:

What is the structural formula of the third member of the alkene family?

EXERCISE-12C | Q 2. (f) | Page 207

The molecules of the alkene family are represented by a general formula CnH2n. Answer the following:

Write the molecular formula of lower and higher homologues of an alkene which contains four carbon atoms.

EXERCISE-12C | Q 3. (a) | Page 207

Distinguish between the saturated hydrocarbon ethane and the unsaturated hydrocarbon ethene by drawing their structural formulae.

EXERCISE-12C | Q 3. (b) | Page 207

Draw the structure of isomers of butene and write their IUPAC names.

EXERCISE-12C | Q 4. | Page 207

Give a balanced equation for the lab. Preparation of ethylene. How is the gas collected?

EXERCISE-12C | Q 5. (a) | Page 207

How is ethene prepared by a dehydrohalogenation reaction? Give an equation and name the products formed.

EXERCISE-12C | Q 5. (b) | Page 207

How is ethene prepared by a dehydration reaction? Give an equation and name the products formed.

EXERCISE-12C | Q 6. (a) | Page 207

Ethylene (ethene), when reacts with halogens (chlorine and bromine) form saturated products. Name them and write balanced equations.

EXERCISE-12C | Q 6. (b) | Page 207

Give the conditions and the main products formed by hydrogenation of ethene. 

EXERCISE-12C | Q 7. (a) | Page 207

Convert ethanol into ethene using a solid dehydrating agent. Give only a balanced equation.

EXERCISE-12C | Q 7. (b) | Page 207

Convert ethanol into ethene using hot conc. H2SO4. Give only a balanced equation.

EXERCISE-12C | Q 8. (a) | Page 207

Write the following property of ethene:

Physical state

EXERCISE-12C | Q 8. (b) | Page 207

Write the following property of ethene: 

Odour 

EXERCISE-12C | Q 8. (c) | Page 207

Write the following property of ethene:

Density as compared to air.

EXERCISE-12C | Q 8. (d) | Page 207

Write the following property of ethene:

Solubility 

EXERCISE-12C | Q 9. (a) | Page 207

How would you convert ethyl bromide into ethene?

EXERCISE-12C | Q 9. (b) | Page 207

How would you convert ethene into 1, 2-dibromoethane?

EXERCISE-12C | Q 9. (c) | Page 207

How would you convert ethene into ethane?

EXERCISE-12C | Q 10. (a) | Page 207

Give the balanced equation when ethene is burnt in excess of oxygen.

EXERCISE-12C | Q 10. (b) | Page 207

Give a balanced equation when ethene reacts with chlorine gas.

EXERCISE-12C | Q 10. (c) | Page 207

Give the balanced equation when ethene combines with hydrogen chloride.

EXERCISE-12C | Q 10. (d) | Page 207

Give the balanced equation when a mixture of ethene and hydrogen is passed over nickel at 200°C.

EXERCISE-12C | Q 11. (a) | Page 207

Give the formula and names of A, B, C and D in the following equation:

\[\ce{CH4 ->[Cl2][-HCl] A ->[Cl2][-HCl] B ->[Cl2][-HCl] C->[Cl2][-HCl] D}\]

EXERCISE-12C | Q 11. (b) | Page 207

Give the formula and names of A, B, C and D in the following equation: 

\[\ce{C2H2 ->[H2] A ->[H2] B ->[Br2][-HBr] C ->[Br2][-HBr] D}\]

EXERCISE-12C | Q 11. (c) | Page 207

Give the formula and names of A, B, C and D in the following equation:

\[\ce{C2H4 + B ->[200^\circ C][Ni] C2H6}\]

EXERCISE-12C | Q 12. (a) | Page 207

Write the name and formula of the product formed in the case below: 

\[\ce{C2H4 + Cl2 -> {..........}}\]

EXERCISE-12C | Q 12. (b) | Page 207

Write the name and formula of the product formed in the case below:

\[\ce{C2H5I + KOH(alc.) ->[\Delta] {...........}}\]

EXERCISE-12C | Q 12. (c) | Page 207

Write the name and formula of the product formed in the case below: 

\[\ce{H2C = CH2 ->[alk.KMnO4] {.........}}\]

EXERCISE-12C | Q 12. (d) | Page 207

Write the name and formula of the product formed in the case below:

\[\ce{H2C = CH2 + HBr -> {...........}}\]

EXERCISE-12C | Q 13. | Page 207

What do you observe when ethene is passed through an alkaline KMnO4 solution?

EXERCISE-12C | Q 14. | Page 207

Name three compounds formed by ethene and give one use of each compound.

EXERCISE-12D [Page 211]

S.P. Singh solutions for कन्साइस केमिस्ट्री [इंग्रजी] इयत्ता १० आयसीएसई0 12 Organic Chemistry EXERCISE-12D [Page 211]

EXERCISE-12D | Q 1. i. | Page 211

What are the sources for alkynes?

EXERCISE-12D | Q 1. ii. | Page 211

Give the general formula of alkynes.

EXERCISE-12D | Q 2. | Page 211

Give an example of isomers shown by triple bond hydrocarbons (alkynes) and write their IUPAC names.

EXERCISE-12D | Q 3. | Page 211

How is ethyne prepared in the laboratory?

  1. Draw a diagram.
  2. Give an equation.
  3. How is pure dry gas collected?
EXERCISE-12D | Q 4. | Page 211

Give the method of preparation of ethyne by 1, 2-dibromoethene.

EXERCISE-12D | Q 5. (a) | Page 211

Name the hydrocarbon which is a tetrahedral molecule.

EXERCISE-12D | Q 5. (b) | Page 211

Name the hydrocarbon which is a planar molecule.

EXERCISE-12D | Q 5. (c) | Page 211

Name the hydrocarbon which is a linear molecule.

EXERCISE-12D | Q 5. (d) | Page 211

Name the hydrocarbon which forms a red precipitate with ammoniacal solution of copper (I) chloride.

EXERCISE-12D | Q 5. (e) | Page 211

Name the hydrocarbon which is known as paraffin.

EXERCISE-12D | Q 5. (f) | Page 211

Name the hydrocarbon which is known as olefin.

EXERCISE-12D | Q 5. (g) | Page 211

Name the hydrocarbon which will give acetylene (ethyne) gas when treated with water.

EXERCISE-12D | Q 6. i. | Page 211

Classify the compound C3H4 as alkanes, alkenes, and alkynes.

EXERCISE-12D | Q 6. ii. | Page 211

Classify the compound C3H8 as alkanes, alkenes, and alkynes.

EXERCISE-12D | Q 6. iii. | Page 211

Classify the compound C5H8 as alkanes, alkenes, and alkynes.

EXERCISE-12D | Q 6. iv. | Page 211

Classify the C3Hcompound as alkanes, alkenes, and alkynes.

EXERCISE-12D | Q 7. (a) | Page 211

Give a chemical test to distinguish between saturated and unsaturated hydrocarbons.

EXERCISE-12D | Q 7. (b) | Page 211

Give a chemical test to distinguish between ethane and ethene.

EXERCISE-12D | Q 7. (c) | Page 211

Give a chemical test to distinguish between ethene (ethylene) and ethyne (acetylene).

EXERCISE-12D | Q 8. | Page 211

Compound X bubbled through bromine dissolved in carbon tetrachloride (CCl4):

\[\begin{array}{cc}
\ce{X ->[Br2/CCl4] CH2Br}\\
\phantom{......}|\\
\phantom{...........}\ce{CH2Br}\\
\end{array}\]

  1. Draw the structure of X.
  2. State your observation during the reaction.
EXERCISE-12D | Q 9. (a) | Page 211

Give a balanced equation for the following conversion.

An alkene to an alkane.

EXERCISE-12D | Q 9. (b) | Page 211

Give a balanced equation for the following conversion.

An alkene to an alcohol.

EXERCISE-12D | Q 9. (c) | Page 211

Give a balanced equation for the following conversion.

An alkyne to an alkene.

EXERCISE-12D | Q 10. (a) | Page 211

Name the products formed and write an equation when ethyne is added to the following in an inert solvent:

Chlorine

EXERCISE-12D | Q 10. (b) | Page 211

Name the products formed and write an equation when ethyne is added to the following in an inert solvent:

Bromine

EXERCISE-12D | Q 10. (c) | Page 211

Name the products formed and write an equation when ethyne is added to the following in an inert solvent:

Iodine

EXERCISE-12D | Q 10. (d) | Page 211

Name the products formed and write an equation when ethyne is added to the following in an inert solvent:

Hydrogen

EXERCISE-12D | Q 10. (e) | Page 211

Name the products formed and write an equation when ethyne is added to the following in an inert solvent:

Excess of hydrochloric acid

EXERCISE-12D | Q 11. | Page 211

Substitution reactions are characteristic reactions of ______.

  • alkynes

  • alkenes

  • alkanes

EXERCISE-12D | Q 12. (a) (i) | Page 211

Write an equation for the laboratory preparation of an unsaturated hydrocarbon from calcium carbide.

EXERCISE-12D | Q 12. (a) (ii) | Page 211

Write an equation for the laboratory preparation of an alcohol from ethyl bromide.

EXERCISE-12D | Q 12. (b) | Page 211

What would you see when ethyne is bubbled through a solution of bromine in carbon tetrachloride?

EXERCISE-12D | Q 12. (c) | Page 211

Name the addition product formed between ethene and water.

EXERCISE-12D | Q 13. (a) | Page 211

Give reasons:

Ethyne is more reactive than ethene.

EXERCISE-12D | Q 13. (b) | Page 211

Give reasons:

Ethene is more reactive than ethane.

EXERCISE-12D | Q 13. (c) | Page 211

Give reasons:

Hydrocarbons are excellent fuels.

EXERCISE-12D | Q 14. (a) (i) | Page 211

Write a balanced equation when butane is burnt in oxygen.

EXERCISE-12D | Q 14. (a) (ii) | Page 211

Write a balanced equation for the following:

Write the equation for the preparation of ethylene from ethyl alcohol.

EXERCISE-12D | Q 14. (b) (i) | Page 211

Convert ethane to acetic acid.

EXERCISE-12D | Q 14. (b) (ii) | Page 211

Convert ethyne to ethane.

EXERCISE-12D | Q 15. (a) | Page 211

Write the equation for the preparation of carbon tetrachloride from methane.

EXERCISE-12D | Q 15. (b) | Page 211

Draw the structural formula of ethyne.

EXERCISE-12D | Q 15. (c) | Page 211

How is the structure of alkynes different from that of alkenes?

EXERCISE-12E [Page 215]

S.P. Singh solutions for कन्साइस केमिस्ट्री [इंग्रजी] इयत्ता १० आयसीएसई0 12 Organic Chemistry EXERCISE-12E [Page 215]

EXERCISE-12E | Q 1. (a) i. | Page 215

What are alcohols?

EXERCISE-12E | Q 1. (a) ii. | Page 215

State the sources of alcohol.

EXERCISE-12E | Q 1. (b) | Page 215

Give the general formula of monohydric alcohol?

EXERCISE-12E | Q 2. (a) | Page 215

Give the dot diagram of the first member of the alcohol.

EXERCISE-12E | Q 2. (b) | Page 215

Give the abbreviated formula of the third member of the alcohol.

EXERCISE-12E | Q 2. (c) | Page 215

Give the structure of the second member of the alcohol group.

EXERCISE-12E | Q 2. (d) | Page 215

Give the structure of alcohol with 4 carbon atoms.

EXERCISE-12E | Q 3. (a) | Page 215

State the method of preparation of ethanol by hydrolysis of ethene.

EXERCISE-12E | Q 3. (b) | Page 215

State the method of preparation of ethanol by hydrolysis of ethyl bromide.

EXERCISE-12E | Q 4. | Page 215

Haloalkanes react with alkalies to produce alcohol. Give the equation for the preparation of the second member of the homologous series of alcohol. State under what condition the reaction occurs.

EXERCISE-12E | Q 5. (a) | Page 215

How do the boiling point and melting point change in the homologous series of alcohols?

EXERCISE-12E | Q 5. (b) (c) | Page 215

Name the product formed when ethanol reacts with acetic acid. Give an equation. What is the name given to this type of reaction?

EXERCISE-12E | Q 6. (a) | Page 215

Complete and balance the following equation. State the condition wherever necessary.

\[\begin{array}{cc}
\ce{CH}\phantom{..............................}\\
\ce{|||\phantom{..}+ H2 -> \underline{}\underline{}\underline{}\underline{} + H2 -> \underline{}\underline{}\underline{}\underline{}}\\
\ce{CH}\phantom{..............................}
\end{array}\]

EXERCISE-12E | Q 6. (b) | Page 215

Complete and balance the following equation. State the condition wherever necessary.

\[\ce{C2H4 + Br2 -> \underline{\phantom{........}}}\]

EXERCISE-12E | Q 6. (c) | Page 215

Complete and balance the following equation. State the condition wherever necessary.

\[\ce{C2H4 + HCl -> \underline{\phantom{.......}}}\]

EXERCISE-12E | Q 6. (d) | Page 215

Complete and balance the following equation. State the condition wherever necessary.

\[\ce{CaC2 + H2O -> \underline{\phantom{.........}}}\]

EXERCISE-12E | Q 6. (e) | Page 215

Complete and balance the following equation. State the condition wherever necessary.

\[\ce{C2H2 + Br2 -> \underline{\phantom{........}}}\]

EXERCISE-12E | Q 6. (f) | Page 215

Complete and balance the following equation. State the condition wherever necessary.

\[\ce{C2H5OH ->[{[O]}][K2Cr2O7] \underline{\phantom{......}}}\]

EXERCISE-12E | Q 7. | Page 215

What is the effect of ethanol on the human body?

EXERCISE-12E | Q 8. (a) | Page 215

How is the absolute alcohol obtained?

EXERCISE-12E | Q 8. (b) | Page 215

How is the spurious alcohol obtained?

EXERCISE-12E | Q 8. (c) | Page 215

How is the methylated spirit obtained?

EXERCISE-12E | Q 9. (a) | Page 215

Name the product formed and give the appropriate chemical equation for the following:

Sodium reacting with ethyl alcohol.

EXERCISE-12E | Q 9. (b) | Page 215

Name the product formed and give an appropriate chemical equation for the following:

Ethanol oxidised by acidified potassium dichromate.

EXERCISE-12E | Q 10. (a) | Page 215

Give the trivial (common) name and IUPAC name of the following:

C3H6

EXERCISE-12E | Q 10. (b) | Page 215

Give the trivial (common) name and IUPAC name of the following:

C2H4

EXERCISE-12E | Q 10. (c) | Page 215

Give the trivial (common) name and IUPAC name of the following:

C2H2

EXERCISE-12E | Q 10. (d) | Page 215

Give the trivial (common) name and the IUPAC name of the following:

CH3OH

EXERCISE-12E | Q 10. (e) | Page 215

Give the trivial (common) name and the IUPAC name of the following:

C2H5OH

EXERCISE-12E | Q 11. | Page 215

Ethanol can be oxidized to ethanoic acid. Write the equation and name the oxidizing agent.

EXERCISE-12E | Q 12. (a) | Page 215

Name an organic compound which is used for illuminating country houses.

EXERCISE-12E | Q 12. (b) | Page 215

Name an organic compound which is used for making a household plastic material.

EXERCISE-12E | Q 12. (c) | Page 215

Name an organic compound which is called ‘wood spirit’.

EXERCISE-12E | Q 12. (d) | Page 215

Name an organic compound which is poisonous and contains OH group.

EXERCISE-12E | Q 12. (e) | Page 215

Name an organic compound which is consumed as a drink.

EXERCISE-12E | Q 12. (f) | Page 215

Name an organic compound which is used in a thermometer.

EXERCISE-12E | Q 12. (g) | Page 215

Name an organic compound which is a solvent for gums and resins.

EXERCISE-12E | Q 12. (h) | Page 215

Name an organic compound which is dehydrated to produce ethene.

EXERCISE-12E | Q 13. (a) | Page 215

Ethanol can be converted into ethene which can be changed into ethane. Choose the correct word or phrase from the options to complete the following sentence.

The conversion of ethanol into ethene is an example of ______.

  • dehydration

  • dehydrogenation

EXERCISE-12E | Q 13. (b) | Page 215

Ethanol can be converted into ethene which can be changed into ethane. Choose the correct word or phrase from the options to complete the following sentence.

Converting ethanol into ethene requires the use of ______.

  • conc. HCl

  • conc. HNO3

  • conc. H2SO4

EXERCISE-12E | Q 13. (c) | Page 215

Ethanol can be converted into ethene which can be changed into ethane. Choose the correct word or phrase from the options to complete the following sentence.

The conversion of ethene into ethane is an example of ______.

  • hydration

  • hydrogenation

EXERCISE-12E | Q 13. (d) | Page 215

Ethanol can be converted into ethene which can be changed into ethane. Choose the correct word or phrase from the options to complete the following sentence.

The catalyst used in the conversion of ethene to ethane is commonly ______.

  • iron

  • cobalt

  • nickel

EXERCISE-12E | Q 14. (a) | Page 215

Write the equation of the following laboratory preparation:

Ethane from sodium propionate.

EXERCISE-12E | Q 14. (b) | Page 215

Write the equation of the following laboratory preparation: 

Ethene from iodoethane.

EXERCISE-12E | Q 14. (c) | Page 215

Write the equation for the following lab preparation:

Ethyne from calcium carbide.

EXERCISE-12E | Q 14. (d) | Page 215

Write the equation for the following lab preparation:

Methanol from iodomethane.

EXERCISE-12E | Q 15. (i) | Page 215

Name the compound prepared by the following reaction:

\[\ce{C2H5COONa +NaOH ->}\] 

EXERCISE-12E | Q 15. (ii) | Page 215

Name the compound prepared by the following reaction:

\[\ce{CH3I + 2H ->}\]

EXERCISE-12E | Q 15. (iii) | Page 215

Name the compound prepared by the following reaction:

\[\ce{C2H5Br + KOH (alcoholic solution) ->}\]

EXERCISE-12E | Q 15. (iv) | Page 215

Name the compound prepared by the following reaction:

\[\ce{CO + 2H2 (Zinc oxide catalyst) ->}\]

EXERCISE-12E | Q 15. (v) | Page 215

Name the compound prepared by the following reaction:

\[\ce{CaC2 + 2H2O ->}\]

EXERCISE-12E | Q 16. (a) | Page 215

Write the equation for the following reaction:

Calcium carbide and water

EXERCISE-12E | Q 16. (b) | Page 215

Write the equation for the following reaction:

Ethene and water (steam)

EXERCISE-12E | Q 16. (c) | Page 215

Write the equation for the following reaction:

Bromoethane and an aqueous solution of sodium hydroxide.

EXERCISE-12F [Pages 217 - 218]

S.P. Singh solutions for कन्साइस केमिस्ट्री [इंग्रजी] इयत्ता १० आयसीएसई0 12 Organic Chemistry EXERCISE-12F [Pages 217 - 218]

EXERCISE-12F | Q 1. i. | Page 217

What are carboxylic acids?

EXERCISE-12F | Q 1. ii. | Page 217

Give the general formula of carboxylic acids.

EXERCISE-12F | Q 2. (a) | Page 217

Write the names of the first three members of the carboxylic acid series.

EXERCISE-12F | Q 2. (b) | Page 217

Write the names of three compounds which can be oxidised directly or in stages to produce acetic acid.

EXERCISE-12F | Q 3. (a) | Page 217

Give the structural formulae of acetic acid.

EXERCISE-12F | Q 3. (b) | Page 217

IUPAC name of acetic acid.

EXERCISE-12F | Q 3. (c) | Page 217

What is glacial acetic acid?

EXERCISE-12F | Q 4. | Page 217

Vinegar is greyish in colour with a particular taste. Explain.

EXERCISE-12F | Q 5. (a) | Page 217

Vinegar is prepared by the bacterial oxidation of ______.

EXERCISE-12F | Q 5. (b) | Page 217

The organic acid present in vinegar is ______.

EXERCISE-12F | Q 5. (c) | Page 217

The next higher homologue of ethanoic acid is ______.

EXERCISE-12F | Q 6. (a) | Page 218

How is acetic acid prepared from ethanol?

EXERCISE-12F | Q 6. (b) | Page 218

How is acetic acid prepared from acetylene?

EXERCISE-12F | Q 7. (a) | Page 218

What do you notice when acetic acid reacts with litmus?

EXERCISE-12F | Q 7. (b) | Page 218

What do you notice when acetic acid reacts with metals?

EXERCISE-12F | Q 7. (c) | Page 218

What do you notice when acetic acid reacts with alkalies?

EXERCISE-12F | Q 7. (d) | Page 218

What do you notice when acetic acid reacts with alcohol?

EXERCISE-12F | Q 8. (a) | Page 218

What do you notice when acetic acid reacts with metals?

EXERCISE-12F | Q 8. (b) | Page 218

What do you notice when acetic acid reacts with metals?

EXERCISE-12F | Q 8. (c) | Page 218

Acetic acid is a typical acid. Write one equation in case of its reactions with a carbonate.

EXERCISE-12F | Q 8. (d) | Page 218

Acetic acid is a typical acid. Write one equation in case of its reactions with a bicarbonate.

EXERCISE-12F | Q 9. (a) | Page 218

What do you observe when acetic acid is added to sodium bicarbonate?

EXERCISE-12F | Q 9. (b) | Page 218

What do you observe when acetic acid is added to ethyl alcohol in the presence of sulphuric acid?

EXERCISE-12F | Q 9. (c) | Page 218

What do you observe when acetic acid is added to a neutral FeCl3 solution?

EXERCISE-12F | Q 10. (a) | Page 218

Name the compound formed when acetic acid and ethanol react together.

EXERCISE-12F | Q 10. (b) | Page 218

Name the reducing agent used to convert acetic acid into ethanol.

EXERCISE-12F | Q 10. (c) | Page 218

Name the substance used to change acetic acid to acetic anhydride?

MISCELLANEOUS [Pages 218 - 219]

S.P. Singh solutions for कन्साइस केमिस्ट्री [इंग्रजी] इयत्ता १० आयसीएसई0 12 Organic Chemistry MISCELLANEOUS [Pages 218 - 219]

MISCELLANEOUS | Q 1. (a) | Page 218

Which of the following statement is wrong about alkanes?

  • They are all saturated hydrocarbons.

  • They can undergo addition as well as substitution reaction.

  • They are almost non-polar in nature.

  • On complete combustion, they give out carbon dioxide and water.

MISCELLANEOUS | Q 1. (b) | Page 218

The organic compound obtained as the end product of the fermentation of a sugar solution is ______.

  • Methanol

  • Ethanol

  • Ethane

  • Methanoic acid

MISCELLANEOUS | Q 1. (c) | Page 218

Find the odd one out and explain:

  • C3H8

  • C5H10

  • C2H6

  • CH4

MISCELLANEOUS | Q 2. (a) | Page 218

Give the chemical equation for the laboratory preparation of methane from sodium acetate.

MISCELLANEOUS | Q 2. (b) | Page 218

Give the chemical equation for the reaction of one mole of ethene with one mole of chlorine gas.

MISCELLANEOUS | Q 2. (c) | Page 218

Give the chemical equation for the preparation of ethyne from 1, 2-dibromoethane.

MISCELLANEOUS | Q 3. (a) | Page 218

State how the following conversion can be carried out:

Ethyl chloride to Ethyl alcohol.

MISCELLANEOUS | Q 3. (b) | Page 218

State how the following conversion can be carried out:

Ethyl chloride to Ethene.

MISCELLANEOUS | Q 3. (c) | Page 218

State how the following conversions can be carried out:

Ethene to Ethyl alcohol.

MISCELLANEOUS | Q 3. (d) | Page 218

State how the following conversion can be carried out:

Ethyl alcohol to ethene.

MISCELLANEOUS | Q 4. (a) | Page 218

Define isomerism.

MISCELLANEOUS | Q 4. (b) | Page 218

Give the IUPAC name of the isomer C4H10 which has a branched-chain.

MISCELLANEOUS | Q 5. | Page 218

A compound X when treated with an organic acid Y (having vinegar-like smell) in the presence of the acid Z, forms a compound P which has a fruity smell.

  1. Identify X, Y and Z
  2. Write the structural formula of X and Y.
  3. What type of compound is P?
  4. Name the above reaction.
  5. If compounds X and Y both have 2 carbon atoms. Write the reaction.
MISCELLANEOUS | Q 6. (a) | Page 218

Write the equation of ethyl bromide with aqueous NaOH.

MISCELLANEOUS | Q 6. (b) | Page 218

Write the equation of ethyl bromide with alcoholic NaOH.

2010

MISCELLANEOUS | Q (a) | Page 218

An organic compound undergoes addition reactions and gives a red colour precipitate with ammoniacal cuprous chloride. Therefore, the organic compound could be ______.

  • Ethane

  • Ethene

  • Ethyne 

  • Ethanol

MISCELLANEOUS | Q (b) | Page 218

An organic weak acid is ______.

  • Formic acid

  • Sulphuric acid

  • Sulphuric base

  • Hydrochloric acid

  • Nitric acid

MISCELLANEOUS | Q (c) | Page 218

The organic compound mixed with ethanol to make it spurious is ______.

  • Methanol

  • Methanoic acid

  • Methanal 

  • Ethanoic acid

MISCELLANEOUS | Q (d) (i) | Page 218

Draw the structural formula for the following:

Ethanoic acid

MISCELLANEOUS | Q (d) (ii) | Page 218

Draw the structural formula for the following:

But-2-yne

MISCELLANEOUS | Q (e) | Page 218

Compound A is bubbled through bromine dissolved in carbon tetrachloride, and the product is CH2Br – CH2Br.
\[\ce{A ->[Br2/CCl4] CH2Br - CH2Br}\]

  1. Draw the structural formula of A.
  2. What type of reaction has A undergone?
  3. What is your observation?
  4. Name (not formula) the compound formed when steam reacts with A in the presence of phosphoric acid.
  5. What is the procedure for converting the product of (iv) back to A?

2011

MISCELLANEOUS | Q (a) | Page 218

The functional group present in acetic acid is ______.

  • Ketonic \[\begin{array}{cc}
    \backslash\phantom{.......}\\
    \ce{C = O}\\
    /\phantom{.......}\\
    \end{array}\]

  • Hydroxyl (–OH)

  • Aldehydic (–CHO)

  •  Carboxyl (–COOH)

MISCELLANEOUS | Q (b) | Page 219

The unsaturated hydrocarbons undergo ______.

  • a substitution reaction

  • an oxidation reaction

  • an addition reaction

  • none of the above

  • redox reaction

MISCELLANEOUS | Q (c) | Page 219

The number of C-H bonds in an ethane molecule is ______.

  • Four

  • Six

  • Eight

  • Ten

Choose the correct word/phrase from within the options to complete the following sentences:

MISCELLANEOUS | Q (d) (i) | Page 219

The catalyst used for the conversion of ethane to ethane is commonly ______.

  • nickel

  • iron

  • cobalt

MISCELLANEOUS | Q (d) (ii) | Page 219

When acetaldehyde is oxidized with acidified potassium dichromate, it forms ______.

  • ester

  • ethanol

  • acetic acid

MISCELLANEOUS | Q (d) (iii) | Page 219

Ethanoic acid reacts with ethanol in the presence of concentrated H2SO4, so as to form a compound and water. The chemical reaction which takes place is called ______.

  • dehydration

  • hydrogenation

  • esterification

MISCELLANEOUS | Q (d) (iv) | Page 219

Write the equation for the reaction taking place between 1, 2-dibromoethane and alcoholic potassium hydroxide.

MISCELLANEOUS | Q (d) (v) | Page 219

The product formed when ethene gas reacts with water in the presence of sulphuric acid is ______.

  • ethanal

  • ethanol

  • ethanoic acid

MISCELLANEOUS | Q (e) (i) | Page 219

Write a balanced chemical equation for the following:

Monochloroethane is hydrolysed with aqueous KOH.

MISCELLANEOUS | Q (e) (ii) | Page 219

Write a balanced chemical equation for the following:

A mixture of sodalime and sodium acetate is heated.

MISCELLANEOUS | Q (e) (iii) | Page 219

Write a balanced chemical equation for the following:

Ethanol under high pressure and low temperature is treated with acidified potassium dichoromate.

MISCELLANEOUS | Q (e) (iv) | Page 219

Write a balanced chemical equation for the following:

Water is added to calcium carbide.

MISCELLANEOUS | Q (e) (v) | Page 219

Write a balanced chemical equation for the following:

Ethanol reacts with sodium at room temperature.

2012

MISCELLANEOUS | Q (a) (i) | Page 219

Give the structural formula for the following:

Methanoic acid

MISCELLANEOUS | Q (a) (ii) | Page 219

Draw the structural formula for the following compound:

Ethanal

MISCELLANEOUS | Q (a) (iii) | Page 219

Draw the structural formula of ethyne.

MISCELLANEOUS | Q (a) (iv) | Page 219

Draw the structural formula for the following compound:

Acetone

MISCELLANEOUS | Q (a) (v) | Page 219

Give the structural formulae of the following:

2-methyl propane

MISCELLANEOUS | Q (b) (i) | Page 219

From the following organic compounds given below, choose one compound in the given case which relates to the description:

An unsaturated hydrocarbon used for welding purposes.

  • Ethyne

  • Ethanol

  • Acetic acid

  • Ethene

  • Methane

MISCELLANEOUS | Q (b) (ii) | Page 219

From the following organic compounds given below, choose one compound in the given case which relates to the description:

An organic compound whose functional group is carboxyl.

  • Ethyne

  • Ethanol

  • Acetic acid

  • Ethene

  • Methane

MISCELLANEOUS | Q (b) (iii) | Page 219

From the following organic compounds given below, choose one compound in the given case which relates to the description:

A hydrocarbon which on catalytic hydrogenation gives a saturated hydrocarbon.

  • Ethyne

  • Ethanol

  • Acetic acid

  • Ethene

  • Methane

MISCELLANEOUS | Q (b) (iv) | Page 219

From the following organic compounds given below, choose one compound in the given case which relates to the description:

An organic compound used as a thermometric liquid.

  • Ethyne

  • Ethanol

  • Acetic acid

  • Ethene

  • Methane

MISCELLANEOUS | Q (c) (i) | Page 219

Why is pure acetic acid also known as glacial acetic acid?

MISCELLANEOUS | Q (c) (ii) | Page 219

Give a chemical equation for the reaction between ethyl alcohol and acetic acid.

2013

MISCELLANEOUS | Q (a) (i) | Page 219

Give a chemical test to distinguish between ethane gas and ethane gas.

MISCELLANEOUS | Q (a) (ii) | Page 219

Identify the statement that is incorrect about alkanes.

  • They are hydrocarbons.

  • There is a single covalent bond between carbon and hydrogen.

  • They can undergo both substitution as well as addition reactions.

  • On complete combustion they produce carbon dioxide and water.

MISCELLANEOUS | Q (b) (i) | Page 219

Give the structural formulae for the following:

An isomer of n-butane.

MISCELLANEOUS | Q (b) (ii) | Page 219

Give the structural formulae for the following:

2-propanol

2014

MISCELLANEOUS | Q (a) | Page 219

The IUPAC name of acetylene is ______.

  • Propane

  • Propyne

  • Ethane

  • Ethyne

MISCELLANEOUS | Q (b) | Page 219

Name hydrocarbons containing \[\begin{array}{cc}
\ce{O}\\
||\\
- \ce{C} -\\
\end{array}\] functional group.

MISCELLANEOUS | Q (c) | Page 219

Write the equation of the following laboratory preparation:

Ethane from sodium propionate.

MISCELLANEOUS | Q (d) | Page 219

Distinguish between the given pair of compounds using the test given within bracket:

Ethane and ethene (using alkaline potassium permanganate solution).

MISCELLANEOUS | Q (e) (i) | Page 219

Give the structural formula of the following:

Ethanol

MISCELLANEOUS | Q (e) (ii) | Page 219

Give the structural formula of the following:

1-propanal

MISCELLANEOUS | Q (e) (iii) | Page 219

Give the structural formula of the following:

Ethanoic acid

MISCELLANEOUS | Q (e) (iv) | Page 219

Draw the structural diagram of 1, 2 dichloroethane.

MISCELLANEOUS | Q (f) | Page 219

Give a balanced equation for the preparation of ethanol from monochloroethane and aq. sodium hydroxide.

2015

MISCELLANEOUS | Q (a) (i) | Page 219

Give a balanced chemical equation for the ethanoic acid to ethyl ethanoate.

MISCELLANEOUS | Q (a) (ii) | Page 219

Give a balanced chemical equation for the following conversion:

Calcium carbide to ethyne.

MISCELLANEOUS | Q (a) (iii) | Page 219

Give a balanced chemical equation for the following conversion:

Sodium ethanoate to methane.

MISCELLANEOUS | Q (b) (i) | Page 219

Using the structural formula, identify the functional group by circling it:

Dimethyl ether

MISCELLANEOUS | Q (b) (ii) | Page 219

Using the structural formula, identify the functional group by circling it:

Propanone 

MISCELLANEOUS | Q (c) (i) | Page 219

Name the following:

Process by which ethane is obtained from ethene.

MISCELLANEOUS | Q (c) (ii) | Page 219

Name the following:

A hydrocarbon which contributes towards the greenhouse effect.

MISCELLANEOUS | Q (c) (iii) | Page 219

Name the following:

Distinctive reaction that takes place when ethanol is treated with acetic acid.

MISCELLANEOUS | Q (c) (iv) | Page 219

Name the following:

The property of elements by virtue of which atoms of the element can link to each other in the form of a long chain or ring structure.

MISCELLANEOUS | Q (c) (v) | Page 219

Name the following:

Reaction when an alkyl halide is treated with alcoholic potassium hydroxide.

MISCELLANEOUS | Q (d) | Page 219

A hydrocarbon which is a greenhouse gas is ______.

  • Acetylene

  • Ethylene

  •  Ethane

  •  Methane

Solutions for 12: Organic Chemistry

Intext QuestionsIntext QuestionsEXERCISE-12AEXERCISE-12BEXERCISE-12CEXERCISE-12DEXERCISE-12EEXERCISE-12FMISCELLANEOUS
S.P. Singh solutions for कन्साइस केमिस्ट्री [इंग्रजी] इयत्ता १० आयसीएसई0 chapter 12 - Organic Chemistry - Shaalaa.com

S.P. Singh solutions for कन्साइस केमिस्ट्री [इंग्रजी] इयत्ता १० आयसीएसई0 chapter 12 - Organic Chemistry

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Concepts covered in कन्साइस केमिस्ट्री [इंग्रजी] इयत्ता १० आयसीएसई0 chapter 12 Organic Chemistry are Organic Chemistry, Organic Compounds, Organic Compounds vs Inorganic Compounds, Carbon: A Versatile Element, Types of Organic Compounds, Hydrocarbons, Cyclic or Closed Chain or Ring Chain Compounds, Structure of Compounds, Alkyl Group, Functional Group, Homologous Series, Nomenclature, Rules of Nomenclature of Organic Compounds, Structural Formula from IUPAC Name, Types of Structural Isomerism, Isomerism, Alkanes, Isomerism in Alkanes, Occurrence of Methane and Ethane, Structure of Methane, Laboratory Preparation of Methane, Laboratory Preparation of Ethane, Other Methods of Preparation of Methane and Ethane, Physical Properties of Methane and Ethane, Chemical Properties of Methane and Ethane, Uses of Methane and Ethane, Alkenes, Ethene (Ethylene), Preparation of Ethene (Ethylene), Physical Properties of Alkenes, Chemical Properties of Alkenes, Uses of Ethene, Alkynes, Ethyne, Physical Properties of Ethyne, Chemical Properties of Ethyne, Uses of Ethyne, Chemical Tests to distinguish between Alkanes, Alkenes and Alkynes, Alcohols, Industrial Method, Physical Properties of Alcohols, Chemical Properties of Alcohols, Uses of Ethyl Alcohol, Carboxylic Acids, Ethanoic Acid, Physical Properties of Ethanoic Acid, Chemical Properties of Ethanoic Acid, Test of Ethanoic Acid, Uses of Ethanoic Acid, Organic Chemistry, Organic Compounds, Organic Compounds vs Inorganic Compounds, Carbon: A Versatile Element, Types of Organic Compounds, Hydrocarbons, Cyclic or Closed Chain or Ring Chain Compounds, Structure of Compounds, Alkyl Group, Functional Group, Homologous Series, Nomenclature, Rules of Nomenclature of Organic Compounds, Structural Formula from IUPAC Name, Types of Structural Isomerism, Isomerism, Alkanes, Isomerism in Alkanes, Occurrence of Methane and Ethane, Structure of Methane, Laboratory Preparation of Methane, Laboratory Preparation of Ethane, Other Methods of Preparation of Methane and Ethane, Physical Properties of Methane and Ethane, Chemical Properties of Methane and Ethane, Uses of Methane and Ethane, Alkenes, Ethene (Ethylene), Preparation of Ethene (Ethylene), Physical Properties of Alkenes, Chemical Properties of Alkenes, Uses of Ethene, Alkynes, Ethyne, Physical Properties of Ethyne, Chemical Properties of Ethyne, Uses of Ethyne, Chemical Tests to distinguish between Alkanes, Alkenes and Alkynes, Alcohols, Industrial Method, Physical Properties of Alcohols, Chemical Properties of Alcohols, Uses of Ethyl Alcohol, Carboxylic Acids, Ethanoic Acid, Physical Properties of Ethanoic Acid, Chemical Properties of Ethanoic Acid, Test of Ethanoic Acid, Uses of Ethanoic Acid, Organic Chemistry, Organic Compounds, Organic Compounds vs Inorganic Compounds, Carbon: A Versatile Element, Types of Organic Compounds, Hydrocarbons, Cyclic or Closed Chain or Ring Chain Compounds, Structure of Compounds, Alkyl Group, Functional Group, Homologous Series, Nomenclature, Rules of Nomenclature of Organic Compounds, Structural Formula from IUPAC Name, Types of Structural Isomerism, Isomerism, Alkanes, Isomerism in Alkanes, Occurrence of Methane and Ethane, Structure of Methane, Laboratory Preparation of Methane, Laboratory Preparation of Ethane, Other Methods of Preparation of Methane and Ethane, Physical Properties of Methane and Ethane, Chemical Properties of Methane and Ethane, Uses of Methane and Ethane, Alkenes, Ethene (Ethylene), Preparation of Ethene (Ethylene), Physical Properties of Alkenes, Chemical Properties of Alkenes, Uses of Ethene, Alkynes, Ethyne, Physical Properties of Ethyne, Chemical Properties of Ethyne, Uses of Ethyne, Chemical Tests to distinguish between Alkanes, Alkenes and Alkynes, Alcohols, Industrial Method, Physical Properties of Alcohols, Chemical Properties of Alcohols, Uses of Ethyl Alcohol, Carboxylic Acids, Ethanoic Acid, Physical Properties of Ethanoic Acid, Chemical Properties of Ethanoic Acid, Test of Ethanoic Acid, Uses of Ethanoic Acid.

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