Question

Acetone is treated with excess of ethanol in the presence of hydrochloric acid. The product obtained is

A. Aldehyde and Ketone mcq option image
B. Aldehyde and Ketone mcq option image
C. Aldehyde and Ketone mcq option image
D. Aldehyde and Ketone mcq option image  
Answer :   Aldehyde and Ketone mcq option image
Solution :
When carbonyl compounds are treated with alcohol, they form hemiacetal ( hemiketal and acetal/ketal. )
Aldehyde and Ketone mcq solution image
NOTE
Formation of hemiketal is a nucleophilic addition reaction.

Releted MCQ Question on
Organic Chemistry >> Aldehyde and Ketone

Releted Question 1

The reagent with which both acetaldehyde and acetone react easily is

A. Fehling’s reagent
B. Grignard reagent
C. Schiff’s reagent
D. Tollen’s reagent
Releted Question 2

The Cannizzaro reaction is not given by

A. trimethylacetaldehye
B. acetaldehyde
C. benzaldehyde
D. formaldehyde
Releted Question 3

The compound that will not give iodoform on treatment with alkali and iodine is :

A. acetone
B. ethanol
C. diethyl ketone
D. isopropyl alcohol
Releted Question 4

Polarisation of electrons in acrolein may be written as

A. $$\mathop {C{H_2}}\limits^{{\delta ^ - }} = CH - \mathop {CH}\limits^{{\delta ^ + }} = O$$
B. $$\mathop {C{H_2}}\limits^{{\delta ^ - }} = CH - CH = \mathop O\limits^{{\delta ^ + }} $$
C. $$\mathop {C{H_2}}\limits^{{\delta ^ - }} = \mathop {CH}\limits^{{\delta ^ + }} - CH = O$$
D. $$\mathop {C{H_2}}\limits^{{\delta ^ + }} = CH - CH = \mathop O\limits^{{\delta ^ - }} $$

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Aldehyde and Ketone


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