Step 1: Geranial and Neral.
Geranial and Neral are indeed geometrical isomers of citral, as they differ only in the orientation of the double bond at the aldehyde group. Hence, statement (A) is correct.
Step 2: Formation of Geranic acid.
Citral, on heating with potassium hydrogen sulfate, undergoes dehydration to form geranic acid, so statement (B) is also correct.
Step 3: Formation of 6-methylhept-5-en-2-one.
Citral does not form 6-methylhept-5-en-2-one when treated with potassium carbonate, making statement (C) incorrect.
Step 4: Oxidation to Laevolic acid.
On oxidation with silver oxide, citral undergoes cleavage to form Laevolic acid, making statement (D) correct.
Final Answer: \[ \boxed{\text{(A), (B) and (D) only}} \]
Arrange the following set of carbocations in order of decreasing stability.
Choose the correct answer from the options given below:
Match List-I with List-II and choose the correct answer:
Match List-I with List-II:
Who said this sentence –
Match List-I with List-II and choose the correct answer:
Match List-I with List-II and choose the correct answer: