Amongst the following alcohols,which would react fastest with conc. $HCl$ and $ZnCl_2$?

Which of the following is incapable of showing the iodoform test?

Consider the following alcohols. The order of decreasing reactivities of these alcohols towards substitution with $HBr$ is:
$(I)$ $C_6H_5CH_2OH$
$(II)$ $p-NO_2-C_6H_4CH_2OH$
$(III)$ $p-CH_3O-C_6H_4CH_2OH$
$(IV)$ $p-Br-C_6H_4CH_2OH$

An alcohol $X$ $(C_5H_{12}O)$ on dehydration gives $Y$ (major product). Reaction of $Y$ with $HBr$ gave $Z$ ($C_5H_{11}Br$,major product). $Z$ undergoes nucleophilic substitution in two steps. What are $X$ and $Y$?

What is the product formed when phenylmagnesium bromide reacts with methanol?

When a Grignard reagent reacts with $(B)$,product $(D)$ is obtained. Reactant $(A)$ of the above reaction is:
$(A)$ $\xrightarrow{PBr_3} (C)$ $\xrightarrow{Mg, \text{ether}} \text{Grignard reagent}$
$(A) \xrightarrow{Na_2Cr_2O_7, H_2SO_4} (B)$
$\text{Grignard reagent} + (B) \to (D) \xrightarrow{H_3O^\oplus} (3,4-\text{dimethylhexan-3-ol})$