The reaction involves the Grignard reagent (\(RMgX\)) reacting with dry \(CO_2\) in the presence of ether to form a product denoted as \(Y\). This intermediate product is then treated with water and acid (\(H_3O^+\)) to eventually yield a carboxylic acid (\(RCOOH\)).
The key reactions occur as follows:
Thus, the correct identity for \(Y\) is the carboxylate salt, which matches the option: \(RCOO-Mg^+X\).

(i) Explain Aldol condensation with example.
(ii) How are the following conversions achieved:
(a) Benzene Benzaldehyde, (b) Ethanoic acid ethanol.
Given below are two statements:
Statement I: Transfer RNAs and ribosomal RNA do not interact with mRNA.
Statement II: RNA interference (RNAi) takes place in all eukaryotic organisms as a method of cellular defence.
In the light of the above statements, choose the most appropriate answer from the options given below:
Aldehydes, Ketones, and Carboxylic Acids are carbonyl compounds that contain a carbon-oxygen double bond. These organic compounds are very important in the field of organic chemistry and also have many industrial applications.
Aldehydes are organic compounds that have the functional group -CHO.
Preparation of Aldehydes
Acid chlorides are reduced to aldehydes with hydrogen in the presence of palladium catalyst spread on barium sulfate.
Ketones are organic compounds that have the functional group C=O and the structure R-(C=O)-R’.
Preparation of Ketones
Acid chlorides on reaction with dialkyl cadmium produce ketones. Dialkyl cadmium themselves are prepared from Grignard reagents.
Carboxylic acids are organic compounds that contain a (C=O)OH group attached to an R group (where R refers to the remaining part of the molecule).
Preparation of Carboxylic Acids
Primary alcohols are readily oxidized to carboxylic acids with common oxidizing agents such as potassium permanganate in neutral acidic or alkaline media or by potassium dichromate and chromium trioxide in acidic media.