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कर्नाटक बोर्ड पी.यू.सी.पीयूसी विज्ञान 2nd PUC Class 12

Alkenes and carbonyl compounds , both contain a π bond but alkenes show electrophilic addition reactions whereas carbonyl compounds show nucleophilic addition reactions. Explain.

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प्रश्न

Alkenes   and carbonyl compounds , both contain a π bond but alkenes show electrophilic addition reactions whereas carbonyl compounds show nucleophilic addition reactions. Explain.

टीपा लिहा
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उत्तर

Carbonyl group is polar in nature. Due to larger electronegativity of oxygen as compared to carbon, carbon acquires partial positive charge while O acquires partial negative charge.

Because of slight positive charge on C atom, it is attacked by nucleophiles and, therefore, undergoes nucleophilic addition reaction.

Ethylenic double bond is a non-polar bond and is a source of electrons. Therefore, it is attacked by electrophiles and undergoes electrophilic addition reactions.

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पाठ 12: Aldehydes, Ketones and Carboxylic Acids - Multiple Choice Questions (Type - I) [पृष्ठ १७३]

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एनसीईआरटी एक्झांप्लर Chemistry Exemplar [English] Class 12
पाठ 12 Aldehydes, Ketones and Carboxylic Acids
Multiple Choice Questions (Type - I) | Q 31 | पृष्ठ १७३

संबंधित प्रश्‍न

Arrange the following in the increasing order of their reactivity towards nucleophilic addition reaction:

C6H5COCH3, CH3-CHO, CH3COCH3


Draw the structure of the semicarbazone of ethanal.


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.


Predict the product of the following reaction:


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

Cyanohydrin


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

Hemiacetal


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

Bromobenzene to 1-Phenylethanol


Write the structure of Phenylmethanamine.


What are amines?


How will you convert benzoic acid to m-bromobenzoic acid?


Paraldehyde is formed as a result of polymerisation:-


Which among the following is most reactive to give nucleophilic addition?


What is the action of sodium hypoiodite on acetone?


The following questions are case-based questions. Read the passage carefully and answer the questions that follow:

The carbon-oxygen double bond is polarised in aldehydes and ketones due to higher electronegativity of oxygen relative to carbon. Therefore, they undergo nucleophilic addition reactions with a number of nucleophiles such as HCN, NaHSO3, alcohols, ammonia derivatives and Grignard reagents. Aldehydes are easily oxidised by mild oxidising agents as compared to ketones. The carbonyl group of carboxylic acid does not give reactions of aldehydes and ketones. Carboxylic acids are considerably more acidic than alcohols and most of simple phenols.

Answer the following:

(a) Write the name of the product when an aldehyde reacts with excess alcohol in the presence of dry HCl. (1)

(b) Why carboxylic acid is a stronger acid than phenol? (1)

(c) (i) Arrange the following compounds in increasing order of their reactivity towards CH3MgBr: (1)

CH3CHO, \[\begin{array}{cc}
\ce{(CH3)3C-C-CH3}\\
\phantom{....}||\\
\phantom{....}\ce{O}
\end{array}\],  \[\begin{array}{cc}
\ce{CH3-C-CH3}\\
||\\
\ce{O}
\end{array}\]

(ii) Write a chemical test to distinguish between propanal and propanone. (1)

OR

(c) Write the main product in the following: (2)

(i)
(ii)

Draw structure of the following derivative.

The ethylene ketal of hexane-3-one


Draw structure of the following derivative.

Acetaldehydedimethylacetal


Draw structure of the following derivative:

Acetaldehydedimethylacetal


Draw structure of the following derivative.

The ethylene ketal of hexan-3-one


Draw structure of the following derivative.

The ethylene ketal of hexan-3-one


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