Carboxylic Acids and Derivatives

Consider the following reaction scheme and choose the correct option(s) for the major products Q, R and S.

In the following reactions, P, Q, R, and S are the major products.

The correct statement about P, Q, R, and S is

In the following reactions, P, Q, R, and S are the major products.

The correct statement(s) about P, Q, R, and S is(are)

Considering the reaction sequence given below, the correct statement(s) is(are)

Considering the following reaction sequence, the correct statement(s) is(are)

Two statements are given belwo :

Statement I : The melting point of monocarboxylic acid with even number of carbon atoms is higher than that of with odd number of carbon atoms acid immediately below and above it in the series.

Statement II : The solubility of monocarboxylic acids in water decreases with increase in molar mass.

Choose the most appropriate option :

Hex-4-ene-2-ol on treatment with PCC gives 'A'. 'A' on reaction with sodium hypoiodite gives 'B', which on further heating with soda lime gives 'C'. The compound 'C' is

The reaction of $\mathrm{R\text{-}\overset{\displaystyle O}{\overset{\|}{C}}\text{-}NH_2}$ with bromine and KOH gives $\mathrm{RNH_2}$ as the end product. Which one of the following is the intermediate product formed in this reaction ?

In the given reaction

'A' can be

The reagent, from the following, which converts benzoic acid to benzaldehyde in one step is

The final product 'A' in the following reaction sequence
$$\mathrm{CH_3CH_2\text{-}\overset{\displaystyle O}{\overset{\|}{C}}\text{-}CH_3\xrightarrow{HCN}?\xrightarrow[\text{Heat}]{95\%\ H_2SO_4}A}$$
is

In the given conversion the compound A is :

Given below are two statements :

Statement I : The esterification of carboxylic acid with an alcohol is a nucleophilic acyl substitution.

Statement II : Electron withdrawing groups in the carboxylic acid will increase the rate of esterification reaction.

Choose the most appropriate option :

Consider the given chemical reaction

Identify the product P.

An organic compound 'A' on reaction with $\mathrm{NH_3}$ followed by heating gives compound B. Which on further strong heating gives compound C ($\mathrm{C_8H_5NO_2}$). Compound C on sequential reaction with ethanolic KOH, alkyl chloride and hydrolysis with alkali gives a primary amine. The compound A is :

In the given reaction

(Where Et is $-\mathrm{C_2H_5}$)

The number of chiral carbon/s in product A is ______.

$[\mathrm{Et\ is\ -C_2H_5}]$

Consider the above reaction and predict the major product.

Find out the major product for the above reaction.

'A' ($\mathrm{C_8H_6Cl_2O}$) reacts with NH$_3$ to give $\mathrm{C_8H_8ClNO}$, which with Br$_2$/NaOH gives 4-chloro-3-methylaniline (shown).

Consider the above reaction, the compound 'A' is :

Major product of the following reaction is

3,3-Dimethylpent-4-enoic acid is treated with I$_2$, NaHCO$_3$.