Q1/10: Which reagent is best for converting a primary alcohol directly to a carboxylic acid?

Q2/10: Tollens reagent test is positive for:

Q3/10: Which compound is formed when acetaldehyde reacts with HCN?

Q4/10: Assertion (A): p-Nitrophenol is more acidic than phenol. Reason (R): Nitro group is electron-withdrawing.

Q5/10: Which alcohol reacts fastest with Lucas reagent?

Q6/10: Denatured alcohol is ethanol made unfit for drinking by adding:

Q7/10: The boiling point of aldehydes and ketones is lower than corresponding alcohols due to:

Q8/10: Decarboxylation of sodium acetate with soda lime yields:

Q9/10: What is the final product when benzene reacts with acetyl chloride in the presence of anhydrous AlCl3?

Q10/10: Stephen reaction is used to prepare:

Q1/10: Ethanoic acid on heating with P2O5 gives:

Q2/10: In Kolbe's reaction, phenol reacts with CO2 and NaOH to mainly form:

Q3/10: Which compound cannot be prepared by Williamson ether synthesis?

Q4/10: Fehlings solution consists of:

Q5/10: Wolff-Kishner reduction uses which reagent?

Q6/10: Which of the following carboxylic acids contains a chiral carbon?

Q7/10: Ethylene glycol on oxidation with periodic acid gives:

Q8/10: Assertion: Benzaldehyde is less reactive than propanal towards nucleophilic addition. Reason: The polarity of the carbonyl group is reduced in benzaldehyde due to resonance.