Ncert Solutions Chemistry Class 12th
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New answer posted
4 months agoContributor-Level 10
This is a Multiple Choice Type Questions as classified in NCERT Exemplar
Correct option: A
The Clemmensen Reduction method is used to reduce a carbonyl group to CH2. Amalgams are a type of reducing agent that has been around for a long time. In the Clemmensen reduction, hydrogen chloride acts as an acid, protonating the ketone and transferring the electrons from the zinc amalgam to the carbon atoms
New answer posted
4 months agoContributor-Level 10
This is a Multiple Choice Type Questions as classified in NCERT Exemplar
Correct option: B
When a primary alcohol, such as Butan-1-ol, reacts with a powerful oxidising agent, such as KMnO4, it produces carboxylic acid, however when a secondary alcohol, such as Butan-2-ol, is oxidised under the pressure of KMnO4, it produces ketone. As a result, option B is right.
New answer posted
4 months agoContributor-Level 10
This is a Multiple Choice Type Questions as classified in NCERT Exemplar
Correct option: C
I2 and NaOH It is an iodoform reaction involving methyl ketones, the solution is the correct reagent. Because the reactants and product have double bonds, double bonds do not work throughout the reaction. There are also ketone and carboxylic groups present. The ketonic group is oxidised under the carboxylic group during the process.
New answer posted
4 months agoContributor-Level 10
This is a Multiple Choice Type Questions as classified in NCERT Exemplar
Correct option: B
The position of a functional group in the same carbon chain differs in positional isomerism. The functional group in the chemical or the unsaturated double or triple bond in the compound can help us figure it out.
New answer posted
4 months agoContributor-Level 10
This is a Multiple Choice Type Questions as classified in NCERT Exemplar
Ans: Correct option: D
New answer posted
4 months agoContributor-Level 10
This is a Multiple Choice Type Questions as classified in NCERT Exemplar
Correct option: B
In KOH adds to the compound
Due to the production of a stable conjugate base after hydronium is removed from phenol, it is more stable than alcohol.
New answer posted
4 months agoContributor-Level 10
This is a Multiple Choice Type Questions as classified in NCERT Exemplar
Correct options: D
Aldehydes without a - hydrogen atom are the subject of Cannizaro's reaction.
Option D, CH3CHO has 3 alpha hydrogen atoms and it does not give Cannizaro's reaction
New answer posted
4 months agoContributor-Level 10
This is a Multiple Choice Type Questions as classified in NCERT Exemplar
Correct option: C
Acetones belong to the ketonic functional category. To distinguish between aldehyde and ketone, utilise Fehling's solution. Carbonyl groups are found in sodium hydrogen sulphite, phenyl hydrazine, and Grignard reagent. Ketones and aromatic aldehydes do not react with Fehling's solution.
New answer posted
4 months agoContributor-Level 10
This is a Multiple Choice Type Questions as classified in NCERT Exemplar
Correct option: B
When phenol reacts with acid chloride in the presence of an alkali, the alkali is pyridine, and the acid chloride is benzoyl chloride, compound C6H5OCOC6H5 is formed. During this process, pyridine is utilised to neutralise 4HCl.
New answer posted
4 months agoContributor-Level 10
This is a Multiple Choice Type Questions as classified in NCERT Exemplar
Correct option: C
Because the phenoxide ion produced is stabilised by resonance, phenol is more acidic than ethanol. When it comes to ethanol, resonance does not help to stabilise the phenoxide ion. The acidity of chloroacetic acid is higher than that of acetic acid. Alcohols and phenols are less acidic than carboxylic acids.
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