The major products U and V in the following reaction are

To identify the major products U and V in the given reaction sequence, we need to analyze both steps of the reaction.
Step 1: The reaction of phenol with isobutyl bromide in the presence of K2CO3 and acetone.
The role of K2CO3 is to deprotonate the phenol, thereby forming phenoxide ion. This ion acts as a nucleophile in an SN2 reaction with isobutyl bromide, resulting in the substitution of the bromide with an isobutyl group on the phenoxide. Thus, compound U is isobutyl phenyl ether.
Step 2: The reaction of phenoxide formed with another alkyl bromide in basic conditions (KOH in benzene).
In the presence of KOH and heat in benzene, the phenoxide ion can undergo another SN2 reaction but this time with the ethylene bromide given. This substitution results in the formation of an ether linkage with ethyl group. The correct product, compound V, would therefore be ethyl isobutyl phenyl ether.
Based on the explanation above, the major products U and V are as shown in the correct image option:

In the following sequence of reactions, what is the end product 'Z'?

Indicate the major product of the following reaction:

The increasing order of basicity of the following compounds is
The products X and Y in the following reaction sequence are
Which one of the following does not lose water even in conc. $H_2SO_4$?
Rank the following anions in order of decreasing nucleophilicity in a polar protic solvent (most $\rightarrow$ least nucleophilic).
The major product in the following reaction is
$RO-CH_2-C\equiv CH \xrightarrow{X} \xrightarrow{Y} RO-CH_2-C\equiv C-CH_2CH_2-Br$
To carry out the above conversion X and Y are respectively
In the following sequence of reactions, what is the end product 'Z'?
