The correct statement regarding a carbonyl compound with a hydrogen atom on its alpha-carbon, is
(1) a carbonyl compound with a hydrogen atom on its alpha-carbon rapidly equilibrates with its corresponding enol and this process is known as aldehyde-ketone equlibration.
(2) a carbonyl compound with a hydrogen atom on its alpha-carbon rapidly eqilibrates with its corresponding enol and this process is known as carbonylation.
(3) a carbonyl compound with a hydrogen atom on its alpha-carbon rapidly eqilibrates with its corresponding enol and this process is known as keto-enol tautomerism.
(4) a carbonyl compound with a hydrogen atom on its alpha-carbon never equilibrates with its corresponding enol
A single compound of the structure is obtained from ozonolysis of which of the following cyclic compounds?
1.
2.
3.
4.
Treatment of cyclopentanone with methyl lithium gives which of the
following species?
1. Cyclopentanonyl anion
2. Cyclopentanonyl cation
3. Cyclopentanonyl radical
4. Cyclopentanonyl biradical
An ester that gets hydrolyzed most easily under alkaline conditions is:
1. | 2. | ||
3. | 4. |
Reaction of a carbonyl compound with one of the following reagents involves nucleophilic
addition followed by the elimination of water. The reagent is:
1. a Grignard reagent
2. hydrazine in presence of feebly acidic solution
3. hydrocyanic acid
4. sodium hydrogen sulphite
The reaction by which benzaldehyde cannot be prepared?
Predicts the products in the given reaction,
1. | 2. | ||
3. | 4. |
Which of the following reactions will not result in the formation of carbon-carbon bonds ?
1. Reimer-Tiemann reaction
2. Cannizaro reaction
3. Wurtz reaction
4. Friedel-Crafts acylation
Which one of the following on treatement with 50% aqueous sodium hydroxide yields the corresponding alcohol and acid ?
(1)
(2)
(3)
(4)