Question
Question: Major product ‘B’ of the given reaction is:  or ketones (in case of secondary alcohol) in the presence of dichloromethane. The reaction proceeds as follows:
Step-2: The ketone formed in step-1 will undergo aldol condensation in the presence of base using following reaction mechanism:
(a) The hydroxide ion present in the medium will extract alpha hydrogen from the ketone to form an enolate. The reaction proceeds as follows:
(b) The enolate will react with another mole of ketone and the attack will take place at the carbonyl centre and an intermediate will be formed. The reaction proceeds as follows:
(c) On acidic workup of the intermediate formed in the previous step, then aldol i.e., beta-hydroxy ketone will be formed. The reaction proceeds as follows:
(d) On heating dehydration of aldol takes place by the removal of water molecules and the final product is formed. The reaction proceeds as follows:
Hence, the major product ‘B’ formed in the given reaction sequence is as follows:
Therefore, option (B) is the correct answer.
Note:
It is important to note that for a compound to undergo aldol condensation, it is mandatory for that compound to have alpha hydrogens i.e., hydrogen atoms bonded to the carbon atom adjacent to the carbonyl group. If there is no alpha hydrogen present within the compound, then the Cannizzaro reaction will take place under the same basic conditions.