What is the Reimer-Tiemann reaction, and what does it produce from phenol?
Alcohols, Phenols and Ethers
Original Khojo Papers practice question — not from a past board paper.
The phenoxide ion left after losing a proton is stabilised by delocalisation of the negative charge over the aromatic ring, so the loss of the proton is easier. The ethoxide ion has no such delocalisation, and the alkyl group is electron-releasing, which intensifies the negative charge and makes ethanol a far weaker acid.
No citable source has been recorded for this record. Treat it as practice material, not as fact.
Electron-withdrawing groups on the ring, as in nitrophenol, increase the acidity further.
From the same topic and chapter, at a similar level.
What is the Reimer-Tiemann reaction, and what does it produce from phenol?
Alcohols, Phenols and Ethers
Describe the Williamson synthesis of ethers and state its limitation.
Alcohols, Phenols and Ethers
How would you distinguish between a primary, a secondary and a tertiary alcohol?
Alcohols, Phenols and Ethers
Distinguish between Schottky and Frenkel defects and state the effect of each on density.
Solid State
What is the van't Hoff factor, and what values does it take for sodium chloride and for acetic acid in benzene?
Solutions
Name the four colligative properties and state what colligative means.
Solutions