Consider the following reaction
The correct statement for product $B$ is It is
kk
So, the correct option is (C): racemic mixture and gives a gas with saturated NaHCO3 solution
The reaction proceeds as follows:
\[ \text{CH}_3\text{CH}_2\text{CHO} + \text{HCHO} \xrightarrow{\text{(i) NaOH, $\Delta$}} \text{CH}_3\text{CH}_2\text{CH(OH)CH}_2\text{CN} \]
In the given reaction, propanal reacts with formaldehyde in the presence of NaOH and heat to form an aldol product. The aldol product undergoes nucleophilic substitution with NaCN, forming a nitrile group.
Upon hydrolysis, the nitrile group is converted into a carboxylic acid, which then undergoes decarboxylation, resulting in a racemic mixture. The carboxylic acid will also release carbon dioxide when reacted with a saturated solution of NaHCO3.
Thus, the correct statement for product B is that it is a racemic mixture and gives a gas with saturated NaHCO3 solution.
Give reasons for the following:
Benzoic acid does not undergo Friedel-Crafts reaction.
(b) HCHO is more reactive than $CH_3\text{CHO towards addition of HCN}$
(c) Vinyl group directly attached with carboxylic acid should decrease the acidity of corresponding carboxylic acid due to resonance, but on the contrary it increases the acidity.
In the given reaction sequence, the structure of Y would be:
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.