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.
An alkyl halide is heated with a sodium alkoxide, and the alkoxide displaces the halide by an SN2 reaction to give the ether. The limitation is that the alkyl halide must be primary; a secondary or tertiary halide undergoes elimination instead and gives an alkene.
No citable source has been recorded for this record. Treat it as practice material, not as fact.
To make an unsymmetrical ether, the bulkier group is therefore taken as the alkoxide.
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
How would you distinguish between a primary, a secondary and a tertiary alcohol?
Alcohols, Phenols and Ethers
Why is phenol more acidic than ethanol?
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