The document discusses several methods for preparing carboxylic acids from other organic compounds. It describes oxidizing alcohols or aldehydes, hydrolyzing nitriles or esters, and carbonating Grignard reagents as common pathways. Specific reaction conditions and reagents are listed for oxidizing primary alcohols, aldehydes, and benzylic alcohols to the corresponding carboxylic acids.
The document discusses several methods for preparing carboxylic acids from other organic compounds. It describes oxidizing alcohols or aldehydes, hydrolyzing nitriles or esters, and carbonating Grignard reagents as common pathways. Specific reaction conditions and reagents are listed for oxidizing primary alcohols, aldehydes, and benzylic alcohols to the corresponding carboxylic acids.
The document discusses several methods for preparing carboxylic acids from other organic compounds. It describes oxidizing alcohols or aldehydes, hydrolyzing nitriles or esters, and carbonating Grignard reagents as common pathways. Specific reaction conditions and reagents are listed for oxidizing primary alcohols, aldehydes, and benzylic alcohols to the corresponding carboxylic acids.
1. Show how you would carry out the following conversion
(i) Cyclohexanol to cyclohexanecarboxylic acid (ii) 2-methyl-2-propanol to 2,2 dimethyl propanoic acid
2. Write equation for the following reactions
(a) Ethanol is heated with acidified K2Cr2O7 (b) Phenylmethanol is heated with acidified Na 2Cr2O7 (c) Ethanal is heated with acidified KMnO4 (d) Benzaldehyde is heated with acidified KMnO4 (e) Ethanenitrile is heated with acidified water (f) Ethyl ethanoate is heated with aqueous NaOH followed by distillation with dilute HCl (g) Prophylbenzene is refluxed with acidified K2Cr2O7 (h) 1,4 dimethylbenzene is refluxed with acidified K2Cr2O7