Ncert Solutions Chemistry Class 12th
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New answer posted
4 months agoContributor-Level 10
This is a Short Answer Type Questions as classified in NCERT Exemplar
When alkaline KMnO4 oxidises compound "B" with compound "A," acid is formed.
New answer posted
4 months agoContributor-Level 10
This is a Short Answer Type Questions as classified in NCERT Exemplar
It's referred to as cross Aldol Condensation.Cross aldol condensation occurs when two separate aldehydes or ketones combine to form a single molecule.
New answer posted
4 months agoContributor-Level 10
This is a Short Answer Type Questions as classified in NCERT Exemplar
ClCH2COOH > FCH2COOH > C6H5CH2COOH > , CH3COOH > CH3CH2OH
When compared to other alcohols, CH3CH2OH is the least acidic. Because of the halogen, FCH2COOH is quite acidic. It is either an electron donating group or an electron receiving group in acidic strength. Acidic strength increases as the number of electron withdrawing groups increases. The acidic strength of electron donating groups diminishes.
New answer posted
4 months agoContributor-Level 10
This is a Short Answer Type Questions as classified in NCERT Exemplar
The electrophile formed when benzene reacts with benzoyl chloride in the presence of anhydrous AlCl3 is benzoylinium cation, and the resultant product is benzophenone. Friedel Crafts acylation reaction is the name for this reaction.
New answer posted
4 months agoContributor-Level 10
Benzal chloride can be made by chlorinating toluene in the presence of sunshine and then using the hydrolysis process to obtain benzaldehyde. This method can be used to make benzaldehyde in a commercial setting.
New answer posted
4 months agoContributor-Level 10
This is a Short Answer Type Questions as classified in NCERT Exemplar
Ans:
A: Ethane-1, 2-dial
B: Benzene-1, 4-carbaldehyde
C: 3-Bromobenzaldehyde
New answer posted
4 months agoContributor-Level 10
This is a Short Answer Type Questions as classified in NCERT Exemplar
(i) 3-Phenylprop-2-ene-1-al.
(ii) Cyclohexanecarbaldehyde
(iii) 3-Oxopentan-1-al
(iv) IUPAC name: But-2-enal
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