Alcohols, Phenols and Ethers

Phthalic acid reacts with resorcinol in the presence of concentrated $\ce{H2SO4}$ to give :

Which one of the following substituents at para-position is most effective in stabilizing the phenoxide ion ($\ce{C6H5O-}$) ?

Which one of the following compounds will not be soluble in sodium bicarbonate ?

Williamson synthesis of ether is an example of :

The compound that does NOT liberate $\ce{CO2}$, on treatment with aqueous sodium bicarbonate solution, is

In the following reaction, the product(s) formed is(are)

The major product(s) of the following reaction is(are)

Match the chemical conversions in List I with the appropriate reagents in List II and select the correct answer using the code given below the lists:

With reference to the scheme given, which of the given statement(s) about T, U, V and W is (are) correct?

The structure of the compound Q is

The major product of the following reaction is

In the reaction $\ce{C6H5-OCH3 ->[HBr]}$ the products are

In the reaction phenol $\xrightarrow{\ce{NaOH(aq)/Br2}}$ the intermediate(s) is(are)

Match the reactions in Column I with appropriate options in Column II.

The correct acidity order of the following is

The structure of the carbonyl compound P is

Match each of the compounds in Column I with its characteristic reaction(s) in Column II.

Match each of the compounds given in Column I with the reaction(s), that they can undergo, given in Column II.

Compound H is formed by the reaction of

The structure of compound I is