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NCERT solutions for केमिस्ट्री पार्ट १ एण्ड २ [अंग्रेजी] कक्षा १२ chapter 8 - Aldehydes, Ketones and Carboxylic Acids [Latest edition]

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NCERT solutions for केमिस्ट्री पार्ट १ एण्ड २ [अंग्रेजी] कक्षा १२ chapter 8 - Aldehydes, Ketones and Carboxylic Acids - Shaalaa.com
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Solutions for Chapter 8: Aldehydes, Ketones and Carboxylic Acids

Below listed, you can find solutions for Chapter 8 of CBSE, Karnataka Board PUC NCERT for केमिस्ट्री पार्ट १ एण्ड २ [अंग्रेजी] कक्षा १२.


Intext QuestionsExercises
Intext Questions [Pages 231 - 254]

NCERT solutions for केमिस्ट्री पार्ट १ एण्ड २ [अंग्रेजी] कक्षा १२ 8 Aldehydes, Ketones and Carboxylic Acids Intext Questions [Pages 231 - 254]

8.1 (i)Page 231

Write the structure of the following compound:

α-Methoxypropionaldehyde

8.1 (ii)Page 231

Write the structure of the following compound:

3-Hydroxybutanal

8.1 (iii)Page 231

Write the structure of the following compound:

2-Hydroxycyclopentane carbaldehyde

8.1 (iv)Page 231

Write the structure of the following compound:

4-Oxopentanal

8.1 (v)Page 231

Write the structure of the following compound:

Di-sec-butyl ketone

8.1 (vi)Page 231

Write the structure of the following compound:

4-Fluoroacetophenone

8.2 (i)Page 234

Write the structure of the product of the following reaction:

8.2 (ii)Page 234

Write the structure of the product of the following reaction:

\[\ce{(C6H5CH2)2 Cd + 2 CH3COCl ->}\]

8.2 (iii)Page 234

Write the structure of the product of the following reaction:

\[\ce{H3C - C ≡ C - H ->[Hg^{2+}, H2SO4]}\]

8.2 (iv)Page 234

Write the structure of the product of the following reaction:

8.3Page 236

Arrange the following compounds in increasing order of their boiling points.

CH3CHO, CH3CH2OH, CH3OCH3, CH3CH2CH3

8.4 (i)Page 243

Arrange the following compound in increasing order of its reactivity in nucleophilic addition reactions.

Ethanal, Propanal, Propanone, Butanone.

Hint: Consider steric effect and electronic effect.

8.4 (ii)Page 243

Arrange the following compound in increasing order of its reactivity in nucleophilic addition reactions.

Benzaldehyde, p-Tolualdehyde, p-Nitrobenzaldehyde, Acetophenone.

Hint: Consider steric effect and electronic effect.

8.5 (i)Page 243

Predict the product of the following reaction:

8.5 (ii)Page 243

Predict the product of the following reaction:

8.5 (iii)Page 243

Predict the product of the following reaction:

\[\begin{array}{cc}
\phantom{..............}\ce{O}\\
\phantom{..............}||\\
\ce{R - CH = CH - CHO + NH2 - C - NH - NH2 ->[H+]}\end{array}\]

8.5 (iv)Page 243

Predict the product of the following reaction:

8.6 (i)Page 245

Give the IUPAC name of the following compound:

PhCH2CH2COOH

8.6 (ii)Page 245

Give the IUPAC name of the following compound:

(CH3)2C=CHCOOH

8.6 (iii)Page 245

Give the IUPAC name of the following compound:

8.6 (iv)Page 245

Give the IUPAC name of the following compound:

8.7 (i)Page 248

Show how the following compound can be converted to benzoic acid.

Ethylbenzene

8.7 (ii)Page 248

Show how the following compound can be converted to benzoic acid.

Acetophenone

8.7 (iii)Page 248

Show how the following compound can be converted to benzoic acid.

Bromobenzene

8.7 (iv)Page 248

Show how the following compound can be converted to benzoic acid.

Phenylethene (Styrene)

8.8 (i)Page 254
Which acid of the pair shown here would you expect to be stronger?

CH3CO2H or CH2FCO2H

8.8 (ii)Page 254

Which acid of the pair shown here would you expect to be stronger?

CH2FCO2H or CH2ClCO2H

8.8 (iii)Page 254

Which acid of the pair shown here would you expect to be stronger?

CH2FCH2CH2CO2H or CH3CHFCH2CO2H

8.8 (iv)Page 254

Which acid of the pair shown here would you expect to be stronger?

Exercises [Pages 255 - 257]

NCERT solutions for केमिस्ट्री पार्ट १ एण्ड २ [अंग्रेजी] कक्षा १२ 8 Aldehydes, Ketones and Carboxylic Acids Exercises [Pages 255 - 257]

8.1 (i)Page 255

What is meant by the following term? Give an example of the reaction in the following case.

Cyanohydrin

8.1 (ii)Page 255

What is meant by the following term? Give an example of the reaction in the following case.

Acetal

8.1 (iii)Page 255

What is meant by the following term? Give an example of the reaction in the following case.

Semicarbazone

8.1 (iv)Page 255

What is meant by the following term? Give an example of the reaction in the following case.

Aldol

8.1 (v)Page 255

What is meant by the following term? Give an example of the reaction in the following case.

Hemiacetal

8.1 (vi)Page 255

What is meant by the following term? Give an example of the reaction in the following case.

Oxime

8.1 (vii)Page 255

What is meant by the following term? Give an example of the reaction in the following case.

Ketal

8.1 (viii)Page 255

What is meant by the following term? Give an example of the reaction in the following case.

Imine

8.1 (ix)Page 255

What is meant by the following term? Give an example of the reaction in the following case.

2, 4-DNP-derivative

8.1 (x)Page 255

What is meant by the following term? Give an example of the reaction in the following case.

Schiff’s base

8.2 (i)Page 255

Name the following compound according to IUPAC system of nomenclature:

CH3CH(CH3)CH2CH2CHO

8.2 (ii)Page 255

Name the following compound according to IUPAC system of nomenclature:

CH3CH2COCH(C2H5)CH2CH2Cl

8.2 (iii)Page 255

Name the following compound according to IUPAC system of nomenclature:

CH3CH=CHCHO

8.2 (iv)Page 255

Name the following compound according to IUPAC system of nomenclature:

CH3COCH2COCH3

8.2 (v)Page 255

Name the following compound according to IUPAC system of nomenclature:

CH3CH(CH3)CH2C(CH3)2COCH3

8.2 (vi)Page 255

Name the following compound according to IUPAC system of nomenclature:

(CH3)3CCH2COOH

8.2 (vii)Page 255

Name the following compound according to IUPAC system of nomenclature:

OHCC6H4CHO-p

8.3 (i)Page 255

Draw the structure of the following compound.

3-Methylbutanal

8.3 (ii)Page 255

Draw the structure of the following compound.

p-Nitropropiophenone

8.3 (iii)Page 255

Write the structure of p-methylbenzaldehyde.

8.3 (iv)Page 255

Draw the structure of the following compound.

4-Methylpent-3-en-2-one

8.3 (v)Page 255

Write the structure of 4-chloropentan-2-one.

8.3 (vi)Page 255

Draw the structure of the following compound.

3-Bromo-4-phenylpentanoic acid

8.3 (vii)Page 2255

Draw the structure of the following compound.

p, p’-Dihydroxybenzophenone

8.3 (viii)Page 255

Draw the structure of the following compound.

Hex-2-en-4-ynoic acid

8.4 (i)Page 255

Write the IUPAC name of the following ketone or aldehyde. Wherever possible, give also the common name.

CH3CO(CH2)4CH3

8.4 (ii)Page 255

Write the IUPAC name of the following ketone or aldehyde. Wherever possible, give also the common name.

CH3CH2CHBrCH2CH(CH3)CHO

8.4 (iii)Page 255

Write the IUPAC name of the following ketone or aldehyde. Wherever possible, give also the common name.

CH3(CH2)5CHO

8.4 (iv)Page 255

Write the IUPAC name of the following ketone or aldehyde. Wherever possible, give also the common name.

Ph-CH=CH-CHO

8.4 (v)Page 255

Write the IUPAC name of the following ketone or aldehyde. Wherever possible, give also the common name.

8.4 (vi)Page 255

Write the IUPAC name of the following ketone or aldehyde. Wherever possible, give also the common name.

PhCOPh

8.5 (i)Page 255

Draw the structure of the given derivative.

The 2, 4-dinitrophenylhydrazone of benzaldehyde

8.5 (ii)Page 255

Draw the structure of the given derivative.

Cyclopropanone oxime

8.5 (iii)Page 255

Draw the structure of the given derivative.

Acetaldehydedimethylacetal

8.5 (iv)Page 255

Draw the structure of the given derivative.

The semicarbazone of cyclobutanone

8.5 (v)Page 255

Draw the structure of the given derivative.

The ethylene ketal of hexan-3-one

8.5 (vi)Page 255

Draw the structure of the given derivative.

The methyl hemiacetal of formaldehyde

8.6 (i)Page 256

Predict the products formed when cyclohexanecarbaldehyde reacts with the following reagents.

PhMgBr and then H3O+

8.6 (ii)Page 256

Predict the products formed when cyclohexanecarbaldehyde reacts with the following reagent.

Tollens’ reagent

8.6 (iii)Page 256

Predict the products formed when cyclohexanecarbaldehyde reacts with the following reagents.

Semicarbazide and weak acid

8.6 (iv)Page 256

Predict the products formed when cyclohexanecarbaldehyde reacts with the following reagents.

Excess ethanol and acid

8.6 (v)Page 256

Predict the products formed when cyclohexanecarbaldehyde reacts with the following reagents.

Zinc amalgam and dilute hydrochloric acid

8.7Page 256

Which of the following compounds would undergo aldol condensation, which the Cannizzaro reaction and which neither? Write the structures of the expected products of aldol condensation and Cannizzaro reaction.

  1. Methanal
  2. 2-Methylpentanal
  3. Benzaldehyde
  4. Benzophenone
  5. Cyclohexanone
  6. 1-Phenylpropanone
  7. Phenylacetaldehyde
  8. Butan-1-ol
  9. 2, 2-Dimethylbutanal
8.8 (i)Page 256

How will you convert ethanal into the following compound?

Butane-1, 3-diol

8.8 (ii)Page 256

How will you convert ethanal into the following compound?

But-2-enal

8.8 (iii)Page 256

How will you convert ethanal into the following compound?

But-2-enoic acid

8.9Page 256

Write structural formulas and names of four possible aldol condensation products from propanal and butanal. In each case, indicate which aldehyde acts as nucleophile and which as electrophile.

8.10Page 256

An organic compound with the molecular formula C9H10O forms 2, 4-DNP derivative, reduces Tollens’ reagent and undergoes Cannizzaro reaction. On vigorous oxidation, it gives 1, 2-benzenedicarboxylic acid. Identify the compound.

8.11Page 256

An organic compound (A) (molecular formula C8H16O2) was hydrolysed with dilute sulphuric acid to give a carboxylic acid (B) and an alcohol (C). Oxidation of (C) with chromic acid produced (B). (C) on dehydration gives but-1-ene. Write equations for the reactions involved.

8.12 (i)Page 256
Arrange the following compounds in increasing order of their property as indicated:

Acetaldehyde, Acetone, Di-tert-butyl ketone, Methyl tert-butyl ketone (reactivity towards HCN)

8.12 (ii)Page 256

Arrange the following compounds in increasing order of their property as indicated:

CH3CH2CH(Br)COOH, CH3CH(Br)CH2COOH, (CH3)2CHCOOH, CH3CH2CH2COOH (acid strength)

8.12 (iii)Page 256

Arrange the following compounds in increasing order of their property as indicated:

Benzoic acid, 4-Nitrobenzoic acid, 3, 4-Dinitrobenzoic acid, 4-Methoxybenzoic acid (acid strength)

8.13 (i)Page 256
Give a simple chemical test to distinguish between the following pair of compounds:

Propanal and Propanone

8.13 (ii)Page 256

Give a simple chemical test to distinguish between the following pair of compounds:

Acetophenone and Benzophenone

8.13 (iii)Page 256

Give a simple chemical test to distinguish between the following pair of compounds:

Phenol and Benzoic acid

8.13 (iv)Page 256

Give a simple chemical test to distinguish between the following pair of compounds:

Benzoic acid and Ethyl benzoate

8.13 (v)Page 256

Give a simple chemical test to distinguish between the following pair of compounds:

Pentan-2-one and Pentan-3-one

8.13 (vi)Page 256

Give a simple chemical test to distinguish between the following pair of compounds:

Benzaldehyde and Acetophenone

8.13 (vii)Page 256

Give a simple chemical test to distinguish between the following pair of compounds:

Ethanal and Propanal

8.14 (i)Page 256

How will you prepare the given compound from benzene? You may use any inorganic reagent and any organic reagent having not more than one carbon atom.

Methyl benzoate

8.14 (ii)Page 256

How will you prepare the given compound from benzene? You may use any inorganic reagent and any organic reagent having not more than one carbon atom.

m-Nitrobenzoic acid

8.14 (iii)Page 256

How will you prepare the given compound from benzene? You may use any inorganic reagent and any organic reagent having not more than one carbon atom.

p-Nitrobenzoic acid

8.14 (iv)Page 256

How will you prepare the given compound from benzene? You may use any inorganic reagent and any organic reagent having not more than one carbon atom.

Phenylacetic acid

8.14 (v)Page 256

How will you prepare the given compound from benzene? You may use any inorganic reagent and any organic reagent having not more than one carbon atom.

p-Nitrobenzaldehyde

8.15 (i)Page 256

How will you bring about the following conversion in not more than two steps?

Propanone to Propene

8.15 (ii)Page 256

How will you bring about the following conversion in not more than two steps?

Benzoic acid to Benzaldehyde

8.15 (iii)Page 256

How will you bring about the following conversion in not more than two steps?

Ethanol to 3-Hydroxybutanal

8.15 (iv)Page 256

How will you bring about the following conversion in not more than two steps?

Benzene to m-Nitroacetophenone

8.15 (v)Page 256

How will you bring about the following conversion in not more than two steps?

Benzaldehyde to Benzophenone

8.15 (vi)Page 256

How will you bring about the following conversion in not more than two steps?

Bromobenzene to 1-Phenylethanol

8.15 (vii)Page 256

How will you bring about the following conversion in not more than two steps?

Benzaldehyde to 3-Phenylpropan-1-ol

8.15 (viii)Page 256

How will you bring about the following conversion in not more than two steps?

Benazaldehyde to α-Hydroxyphenylacetic acid

8.15 (ix)Page 256

How will you bring about the following conversion in not more than two steps?

Benzoic acid to m-Nitrobenzyl alcohol

8.16 (i)Page 256

Describe the following:

Acetylation

8.16 (ii)Page 256

Describe the following:

Cannizzaro reaction

8.16 (iii)Page 256

Describe the following:

Cross aldol condensation

8.16 (iv)Page 256

Describe the following:

Decarboxylation

8.17 (i)Page 257

Complete the synthesis by giving missing starting material, reagent or product.

8.17 (ii)Page 257

Complete the synthesis by giving missing starting material, reagent or product.

8.17 (iii)Page 257

Complete the synthesis by giving missing starting material, reagent or product.

\[\ce{C6H5CHO ->[H2NCONHNH2]}\]

8.17 (iv)Page 257

Complete the synthesis by giving missing starting material, reagent or product.

8.17 (v)Page 257

Complete the synthesis by giving missing starting material, reagent or product.

8.17 (vi)Page 257

Complete the synthesis by giving missing starting material, reagent or product.

8.17 (vii)Page 257

Complete the synthesis by giving missing starting material, reagent or product.

\[\begin{array}{cc}
\ce{C6H5CHO}\phantom{............}\\
\phantom{........}\ce{+\phantom{......}\ce{->[dil.NaOH][\Delta]}}\phantom{...}\\
\ce{CH3CH2CHO}\phantom{............}
\end{array}\]

8.17 (viii)Page 257

Complete the synthesis by giving missing starting material, reagent or product.

\[\ce{CH3COCH2COOC2H5 ->[(i) NaBH4][(ii) H+]}\]

8.17 (ix)Page 257

Complete the synthesis by giving missing starting material, reagent or product.

8.17 (x)Page 257

Complete the synthesis by giving missing starting material, reagent or product.

8.17 (xi)Page 257

Complete the synthesis by giving missing starting material, reagent or product.

8.18 (i)Page 257

Give plausible explanation for the following:

Cyclohexanone forms cyanohydrin in good yield but 2, 2, 6 trimethylcyclohexanone does not.

8.18 (ii)Page 257

Give plausible explanation for the following:

There are two −NH2 groups in semicarbazide. However, only one is involved in the formation of semicarbazones.

8.18 (iii)Page 257

Give plausible explanation for the following:

During the preparation of esters from a carboxylic acid and an alcohol in the presence of an acid catalyst, the water or the ester should be removed as soon as it is formed.

8.19Page 257

An organic compound contains 69.77% carbon, 11.63% hydrogen and rest oxygen. The molecular mass of the compound is 86. It does not reduce Tollens’ reagent but forms an addition compound with sodium hydrogensulphite and give positive iodoform test. On vigorous oxidation it gives ethanoic and propanoic acid. Write the possible structure of the compound.

8.20Page 257

Although phenoxide ion has more number of resonating structures than carboxylate ion, carboxylic acid is a stronger acid than phenol. Give two reasons.

Solutions for 8: Aldehydes, Ketones and Carboxylic Acids

Intext QuestionsExercises
NCERT solutions for केमिस्ट्री पार्ट १ एण्ड २ [अंग्रेजी] कक्षा १२ chapter 8 - Aldehydes, Ketones and Carboxylic Acids - Shaalaa.com

NCERT solutions for केमिस्ट्री पार्ट १ एण्ड २ [अंग्रेजी] कक्षा १२ chapter 8 - Aldehydes, Ketones and Carboxylic Acids

Shaalaa.com has the CBSE, Karnataka Board PUC Mathematics केमिस्ट्री पार्ट १ एण्ड २ [अंग्रेजी] कक्षा १२ CBSE, Karnataka Board PUC solutions in a manner that help students grasp basic concepts better and faster. The detailed, step-by-step solutions will help you understand the concepts better and clarify any confusion. NCERT solutions for Mathematics केमिस्ट्री पार्ट १ एण्ड २ [अंग्रेजी] कक्षा १२ CBSE, Karnataka Board PUC 8 (Aldehydes, Ketones and Carboxylic Acids) include all questions with answers and detailed explanations. This will clear students' doubts about questions and improve their application skills while preparing for board exams.

Further, we at Shaalaa.com provide such solutions so students can prepare for written exams. NCERT textbook solutions can be a core help for self-study and provide excellent self-help guidance for students.

Concepts covered in केमिस्ट्री पार्ट १ एण्ड २ [अंग्रेजी] कक्षा १२ chapter 8 Aldehydes, Ketones and Carboxylic Acids are Nomenclature of Aldehydes and Ketones, Nature of Carbonyl Group, Preparation of Aldehydes and Ketones, Physical Properties of Aldehydes and Ketones, Chemical Reactions of Aldehydes and Ketones - Nucleophilic Addition Reactions, Uses of Aldehydes and Ketones, Nomenclature of Carboxylic Acids, Structure of the Carboxyl group, Methods of Preparation of Carboxylic Acids, Physical Properties of Carboxylic Acids, Uses of Carboxylic Acids, Concepts of Aldehydes, Ketones, and Carboxylic Acids, Preparation of Aldehydes, Preparation of Ketones, Chemical Reactions of Aldehydes and Ketones - Reduction, Chemical Reactions of Aldehydes and Ketones - Oxidation, Chemical Reactions of Aldehydes and Ketones - Reactions Due to α-hydrogen, Chemical Reactions of Aldehydes and Ketones - Other Reactions, Chemical Reactions of Carboxylic Acids - Reactions Involving Cleavege of O-H Bond, Chemical Reactions of Carboxylic Acids - Reactions Involving Cleavege of C-OH Bond, Chemical Reactions of Carboxylic Acids - Reactions Involving –COOH Group, Chemical Reactions of Carboxylic Acids - Substitution Reactions in the Hydrocarbon Part, Structure of the Carbonyl Group, Carboxylic Acids, Overview: Aldehydes, Ketones and Carboxylic Acids, Nomenclature of Aldehydes and Ketones, Nature of Carbonyl Group, Preparation of Aldehydes and Ketones, Physical Properties of Aldehydes and Ketones, Chemical Reactions of Aldehydes and Ketones - Nucleophilic Addition Reactions, Uses of Aldehydes and Ketones, Nomenclature of Carboxylic Acids, Structure of the Carboxyl group, Methods of Preparation of Carboxylic Acids, Physical Properties of Carboxylic Acids, Uses of Carboxylic Acids, Concepts of Aldehydes, Ketones, and Carboxylic Acids, Preparation of Aldehydes, Preparation of Ketones, Chemical Reactions of Aldehydes and Ketones - Reduction, Chemical Reactions of Aldehydes and Ketones - Oxidation, Chemical Reactions of Aldehydes and Ketones - Reactions Due to α-hydrogen, Chemical Reactions of Aldehydes and Ketones - Other Reactions, Chemical Reactions of Carboxylic Acids - Reactions Involving Cleavege of O-H Bond, Chemical Reactions of Carboxylic Acids - Reactions Involving Cleavege of C-OH Bond, Chemical Reactions of Carboxylic Acids - Reactions Involving –COOH Group, Chemical Reactions of Carboxylic Acids - Substitution Reactions in the Hydrocarbon Part, Structure of the Carbonyl Group, Carboxylic Acids, Overview: Aldehydes, Ketones and Carboxylic Acids.

Using NCERT केमिस्ट्री पार्ट १ एण्ड २ [अंग्रेजी] कक्षा १२ solutions Aldehydes, Ketones and Carboxylic Acids exercise by students is an easy way to prepare for the exams, as they involve solutions arranged chapter-wise and also page-wise. The questions involved in NCERT Solutions are essential questions that can be asked in the final exam. Maximum CBSE, Karnataka Board PUC केमिस्ट्री पार्ट १ एण्ड २ [अंग्रेजी] कक्षा १२ students prefer NCERT Textbook Solutions to score more in exams.

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