Special Reactions of Carbonyl Compounds

Compound which gives intramolecular aldol reaction?

Why propanal undergoes oxidation reaction faster than the propanone?

Aldehydes are easily oxidesed than the ketone.

Why aldehydes are easily oxidised compared to ketone?

The reduction of acetone by $\mathrm{Mg}-\mathrm{Hg}$ gives:

Identify the products in the following reaction.

 is

In the given reaction sequence what will be the final product $\text{'}\mathrm{T}\text{'}$?

${\mathrm{C}}_{\text{6}}{\mathrm{H}}_{\text{5}}\text{-CH=O}\stackrel{\text{KCN/Δ}}{\to }\text{R}\stackrel{\text{PCC}}{\to }\text{S}$$\underset{\left(\text{ii}\right) \text{Acidification}}{\overset{\left(\text{i}\right) \text{conc KOH}}{\to }}\text{T}$

Which of the following keto esters is /are not likely to have been prepared by a Claisen condensation?

What is $\mathrm{X}$? 

In the below reaction, which product is formed?

$C_6{H}_{5}CHO+C{H}_{3}COC{H}_3 \begin{array}{c}\stackrel{O{H}^{-}}{\to }\\ ∆\end{array}P$ 

Aldehydes can undergo aldol condensations and Cannizzaro reactions depending upon the reaction conditions.

Product is

. Here [Z] is

In which of the reaction $\mathrm{\alpha },\mathrm{ }\mathrm{\beta }$ -unsaturated aldehyde, ketone or acid is not the main product?

Which of the following named reaction is not used for introducing a - COOH group?

The first two steps of the above set of reactions involve which reaction?

The reaction given below is an example of