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(D) The reaction involves the nucleophilic substitution of an allylic bromide with a phenoxide ion. $1$. The base $(K_2CO_3)$ deprotonates phenol to f

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(D) The reaction involves the nucleophilic substitution of an allylic bromide with a phenoxide ion. $1$. The base $(K_2CO_3)$ deprotonates phenol to form the phenoxide ion $(C_6H_5O^-)$. $2$. The phenoxide ion acts as a nucleophile and attacks the electrophilic carbon of the allylic bromide ($CH_3)_2C=CH-CH_2Br$ via an $S_N2$ mechanism. $3$. The bromide ion is displaced as a leaving group,resulting in the formation of an allyl phenyl ether. $4$. The structure of the product is $(CH_3)_2C=CH-CH_2-O-C_6H_5$.

The major product of the following reaction,if it occurs by $S_N2$ mechanism is :

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