Consider the below reaction,and choose the co | vedclass

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(D) The reaction is an acid-catalyzed dehydration of an alcohol. $1$. The hydroxyl group is protonated by $H_2SO_4$ to form a good leaving group $(-OH

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Compound $A$ will be the major product

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(D) The reaction is an acid-catalyzed dehydration of an alcohol. $1$. The hydroxyl group is protonated by $H_2SO_4$ to form a good leaving group $(-OH_2^+)$. $2$. Water is eliminated to form a stable benzylic carbocation. $3$. $A$ proton is removed from the adjacent carbon to form an alkene. $4$. The resulting alkene can exist as two geometric isomers: $A$ (trans-isomer) and $B$ (cis-isomer). $5$. The trans-isomer $(A)$ is more stable due to reduced steric hindrance compared to the cis-isomer $(B)$. $6$. According to the thermodynamic control of the reaction,the more stable product is formed as the major product. Therefore,compound $A$ is the major product.

Consider the below reaction,and choose the correct statement:

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