Derivatives of Carboxylic Acids

Acetyl bromide reacts with excess of  ${\mathrm{CH}}_3\mathrm{MgI}$ followed by treatment with a saturated solution of  ${\mathrm{NH}}_4\mathrm{Cl}$ gives –

Find the product when POCl₃ reacts with Benzamide:

The product formed when two equivalents of ${\mathrm{CH}}_3\mathrm{MgBr}$ reacts with acetyl chloride followed by hydrolysis is

Compound  can be prepared by the reaction of ________.

Which of the following is by product of saponification :

How many moles of Grignard reagent will be consumed during the following reaction for one mole of the starting compound?

What is the value of $\mathrm{x}+\mathrm{y}=?$

Which of following compound is most reactive towards Nucleophilic substitution reaction?

Product $\mathrm{A}$ is :-

The "saponification value" of an oil or fat is measured in terms of:

Find the number of compounds which can react with odd number of moles of ${\mathrm{CH}}_3\text{COCl}$ /pyridine per mole of it.

(i)



In major products, let the number of $\mathrm{\alpha }-\mathrm{H}$ is X.
(ii)



Let the number of $\mathrm{MeMgBr}$ consumed per molecule is Y.

(iii)



Let the number of organic products formed during this reaction is Z.

Then the sum of  values of  X, Y, Z will be

What is the correct decreasing order of ease of alkaline hydrolysis for the following esters?

$\underset{{\mathrm{C}}_5{\mathrm{H}}_8{\mathrm{O}}_3}{\mathrm{X}} \stackrel{\mathrm{NaOEt}}{\to }\mathrm{Y}\stackrel{{\mathrm{CH}}_3\mathrm{Br}}{\to }\mathrm{Z}\stackrel{{\mathrm{H}}_3{\mathrm{O}}^{+}}{\to }\mathrm{U}\stackrel{∆}{\to }\underset{{\mathrm{C}}_4{\mathrm{H}}_8\mathrm{O}}{\mathrm{P}}+{\mathrm{CO}}_2$

If compound $\mathrm{P}$ gives $2,4$-DNP and iodoform tests both. The possible structures of compound X may be-

Major product of the reaction can be-

${\mathrm{C}\mathrm{H}}_3\mathrm{C}\mathrm{O}\mathrm{C}{\left({\mathrm{C}\mathrm{H}}_3\right)}_3\stackrel{{\mathrm{C}\mathrm{F}}_3{\mathrm{C}\mathrm{O}}_3\mathrm{H}}{\to }$
 

$\mathrm{C}\mathrm{H}\equiv \mathrm{C}\mathrm{H}\stackrel{\mathrm{C}{\mathrm{H}}_3\mathrm{M}\mathrm{g}\mathrm{B}\mathrm{r}\mathrm{ }}{\to }\mathrm{ }\mathrm{ }\stackrel{\mathrm{C}{\mathrm{O}}_2/{\mathrm{H}}_2{\mathrm{O}}^{+}}{\to }\mathrm{ }\mathrm{ }\stackrel{\mathrm{H}\mathrm{g}\mathrm{S}{\mathrm{O}}_4}{\to }\mathrm{ }\mathrm{ }\underset{∆}{\overset{{\mathrm{Ag}}_2\mathrm{O}}{\to }}$

What is the end product of the above sequence of reactions?
 

The product formed when ${\left({\mathrm{CH}}_3\right)}_3\mathrm{CMgCl}$ reacts with ${\mathrm{D}}_2\mathrm{O}$:

The number of compounds that does not contain dicarboxylic acid functional groups. Among the following is:

$\mathrm{i}$. Oxalic acid          $\mathrm{ii}$. Adipic acid
$\mathrm{iii}$. Phthalic acid     $\mathrm{iv}$. Lactic acid
$\mathrm{v}$. Succinic acid     $\mathrm{vi}$. Malonic acid
$\mathrm{vii}$. Benzoic acid    $\mathrm{viii}$. n-Valeric acid

What will be the structure of the major product $\text{'}\mathrm{X}\text{'}$ in the following reaction:

How many of the following are NOT dicarboxylic acids?
i. Oxalic acid          ii. Adipic acid
iii. Phthalic acid     iv. Lactic acid
v. Succinic acid     vi. Malonic acid
vii. Benzoic acid    viii.n-Valeric acid