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Write IUPAC names of the following - Chemistry

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Write IUPAC names of the following

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2-Nitrophenol

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पाठ 11: Alcohols, Phenols and Ethers - Exercises [पृष्ठ २५३]

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बालभारती Chemistry [English] Standard 12 Maharashtra State Board
पाठ 11 Alcohols, Phenols and Ethers
Exercises | Q 6.3 | पृष्ठ २५३

व्हिडिओ ट्यूटोरियलVIEW ALL [3]

संबंधित प्रश्‍न

Explain metamerism with suitable examples of ethers


Write the IUPAC name of the given compound:


Name the following compound according to IUPAC system.


Name the following compound according to IUPAC system.

\[\begin{array}{cc}
\ce{H2C = CH - CH - CH2 - CH2 - CH3}\\
|\phantom{..........}\\
\ce{OH}\phantom{........}
\end{array}\]


Write IUPAC name of the following compound:

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


Write IUPAC name of the following compound:

\[\begin{array}{cc}
\ce{H3C - CH - CH2 - CH - CH - CH2 - CH3}\\
\phantom{}|\phantom{.............}|\phantom{......}|\phantom{.........}\\
\phantom{}\ce{OH}\phantom{..........}\ce{OH}\phantom{...}\ce{C2H5}\phantom{......}
\end{array}\]


Write IUPAC name of the following compound:

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


Write IUPAC name of the following compound:

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


Write IUPAC name of the following compound:


Write IUPAC name of the following compound:


Write IUPAC name of the following compound:


Write IUPAC name of the following compound:

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


Write IUPAC name of the following compound:

C6H5 – O – C7H15(n−)


Write structures of the compounds whose IUPAC names are as follows:

3-Chloromethylpentan-1-ol.


  1. Draw the structures of all isomeric alcohols of molecular formula C5H12O and give their IUPAC names.
  2. Classify the isomers of alcohols in the above question as primary, secondary and tertiary alcohols.

Give IUPAC name of the following ether:

\[\begin{array}{cc}
\ce{C2H5OCH2 - CH - CH3}\\
\phantom{.....}|\\
\phantom{.......}\ce{CH3}
\end{array}\]


Give IUPAC name of the following ether:

CH3OCH2CH2Cl


Give IUPAC name of the following ether:


Ethylidene dichloride when boiled with aqueous solution of NaOH yields _______.

(A) formaldehyde

(B) acetaldehyde

(C) acetone

(D) ethyl methyl ketone


Natalite is a mixture of

(a) diethyl ether and methanol

(b) diethyl ether and ethanol

(c) dimethyl ether and methanol

(d) dimethyl ether and ethanol


Which of the following compounds is NOT prepared by the action of alcoholic NI3 on alkyl halide?

(a) CH3NH2

(b) CH3- CH2- NH2

(c) CH3 - CH2 - CH2 - NH2

(d) (CH3)C- NH2


What is the action of hot HI on it?


How is phenol converted into the following?

Benzene


How is phenol converted into the following?

picric acid


Write the IUPAC name of the following :


What.will be the product fonned when chlorobenzene is heated with sodium metal in the presence of dry ether?


Propanoic acid to ethylamine.


Resorcinol on distillation with zinc dust gives _________.


Write structural formulae for 3-Methoxyhexane


Write structural formula for Methyl vinyl ether.


Write structural formulae for 1-Ethylcyclohexanol.


Write IUPAC name of the following


Write IUPAC name of the following

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


Write IUPAC names of the following


In a carbinol system of nomenclature tert.butyl alcohol is named as _______________


Isopropyl alcohol on oxidation forms:


Give IUPAC names of the following compound:


Give IUPAC names of the following compound:

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


C6H5OCH2CH3 is called:


3-methylphenol is called ____________.


An example of a compound with functional group – O – is ____________.


Butane-2-ol is ____________.


Ethyl alcohol is industrially prepared from ethylene by:


Which of the following compounds is oxidised to prepare methyl ethyl ketone?


HBr reacts fastest with ____________.


n-Propyl alcohol and isopropyl alcohol can be chemically distinguished by which reagent?


Ethylene reacts with Baeyer’s reagent to give ______.


When ethyl alcohol reacts with acetic acid, the products formed are:


1-Propanol and 2-propanol can be best distinguished by:


Which of the following is most acidic?


The IUPAC name of the ether CH2 = CH–CH2OCH3 is:


\[\ce{HC ≡ CH ->[HgSO4][H2SO4] ->[CH3MgBr][H2O] ->[PBr3]}\]


The product of acid catalysed hydration of 2-phenylpropene is:


The heating of phenyl methyl ether with HI produces:


\[\ce{Phenol ->[Zn, dust] 'X' ->[CH3Cl][Anhy. AlCl3] 'Y' ->[Alkaline][KMnO4] 'Z'}\]

The product ‘Z’ is:


IUPAC name of the compound is:

\[\begin{array}{cc}
\ce{CH3-CH-OCH3}\\
|\phantom{....}\\
\ce{CH3}\phantom{..}
\end{array}\]


IUPAC name of m-cresol is ______.


IUPAC name of the compound \[\begin{array}{cc}
\ce{CH3 - CH - OCH3}\\
\phantom{}|\phantom{....}\\
\phantom{}\ce{CH3}\phantom{..}
\end{array}\] is ______.


Give IUPAC name of the compound given below.

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


Which of the following compounds will react with sodium hydroxide solution in water?


What happens when benzene diazonium chloride is heated with water?


Write steps to carry out the conversion of phenol to aspirin.


Explain why p-nitrophenol is more acidic than phenol.


Match the starting materials given in Column I with the products formed by these (Column II) in the reaction with HI.

  Column I   Column II
(i) CH3—O—CH3 (a)
(ii) \[\begin{array}{cc}
\ce{CH3}\phantom{..................}\\
\backslash\phantom{.............}\\
\ce{CH-O-CH3}\\
/\phantom{..............}\\
\ce{CH3}\phantom{..................}
\end{array}\]
(b) \[\begin{array}{cc}
\ce{CH3}\phantom{....}\\
|\phantom{.......}\\
\ce{CH3-C-I + CH3OH}\\
|\phantom{.......}\\
\ce{CH3}\phantom{....}
\end{array}\]
(iii) \[\begin{array}{cc}
\ce{CH3}\phantom{.}\\
|\phantom{....}\\
\ce{H3C-C-O-CH3}\\
|\phantom{....}\\
\ce{CH3}\phantom{..}
\end{array}\]
(c)
(iv) (d) CH3—OH + CH3—I
    (e) \[\begin{array}{cc}
\ce{CH3}\phantom{.....................}\\
\backslash\phantom{.................}\\
\ce{CH-OH + CH3I}\\
/\phantom{.................}\\
\ce{CH3}\phantom{.....................}
\end{array}\]
    (f) \[\begin{array}{cc}
\ce{CH3}\phantom{.....................}\\
\backslash\phantom{.................}\\
\ce{CH-I + CH3OH}\\
/\phantom{.................}\\
\ce{CH3}\phantom{.....................}
\end{array}\]
    (g) \[\begin{array}{cc}
\ce{CH3}\phantom{....}\\
|\phantom{.......}\\
\ce{CH3-C-OH + CH3I}\\
|\phantom{.......}\\
\ce{CH3}\phantom{....}
\end{array}\]

Assertion: Addition reaction of water to but-1-ene in acidic medium yields butan-1-ol.

Reason: Addition of water in acidic medium proceeds through the formation of primary carbocation.


Assertion: IUPAC name of the compound

\[\begin{array}{cc}
\ce{CH3 - CH - O - CH2 - CH2 - CH3}\\  
|\phantom{....................}\\
\ce{CH3}\phantom{.................}
\end{array}\] is 2-Ethoxy-2-methylethane.

Reason: In IUPAC nomenclature, ether is regarded as hydrocarbon derivative in which a hydrogen atom is replaced by —OR or —OAr group [where R = alkyl group and Ar = aryl group]


Assertion: Like bromination of benzene, bromination of phenol is also carried out in the presence of Lewis acid.

Reason: Lewis acid polarises the bromine molecule.


Assertion: Phenol forms 2, 4, 6 – tribromophenol on treatment with \[\ce{Br2}\] in carbon disulphide at 273 K.

Reason: Bromine polarises in carbon disulphide.


Assertion: Phenols give o- and p-nitrophenol on nitration with conc. \[\ce{HNO3}\] and \[\ce{H2SO4}\] mixture.

Reason: –OH group in phenol is o–, p– directing.


Write the IUPAC name of the following compound.


Convert the following:

Ethyl alcohol into ethyl acetate.


Write a chemical reaction for the following conversion:

Acetic acid into ethyl alcohol.


Identify A and B in the following:


How are the following conversions carried out?

Methyl magnesium bromide→2-Methylpropan-2-ol.


Draw structure of the following compound.

2. 5-Diethylphenol


Draw structure of the following compound.

Prop-2-en-1-ol


Give the structures of Thiosulphuric acid and Peroxy monosulphuric acid.


The IUPAC name of is ______.


Write IUPAC name of the following compound:

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


Write the IUPAC name.

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


Write IUPAC name of the following compound:

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


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