Chemistry Alkyl Halides BUMHS 2024
PMDC Verified Question 8 of 13
The procedure for the preparation of ethers in which an alcohol is first allowed to react with metallic sodium is called:
A
Tollen's synthesis
B
Fehling's synthesis
C
Williamson's synthesis
D
Grignard's synthesis
Tap any option to test your recall and reveal the step-by-step Propolis autopsy.

Propolis Cognitive Error Autopsy

Official Correct Choice:
Option C: Williamson's synthesis
Concept:

The standard laboratory method for creating asymmetrical or symmetrical ethers involves an \( S_N2 \) reaction between an alkoxide ion and an alkyl halide.

Solution:

  • Step 1: An alcohol (\( R-OH \)) is reacted with an active metal like sodium (\( Na \)) to produce sodium alkoxide (\( R-O^-Na^+ \)), releasing hydrogen gas.
  • Step 2: This strong nucleophile (alkoxide) is then reacted with a primary alkyl halide (\( R'-X \)).
  • The alkoxide attacks the alkyl halide, displacing the halogen to form an ether (\( R-O-R' \)).
  • This two-step protocol was developed by Alexander Williamson and is universally known as the Williamson ether synthesis.


Why other options are incorrect:

  • Options A & B: Tollen's and Fehling's reagents are used to test for the presence of aldehydes.
  • Option D: Grignard synthesis uses magnesium to create organometallic reagents for carbon-carbon bond formation.

Quality & Fidelity Assurance: Every question on BeambePrep is rigorously curated against the official PMDC syllabus with zero filler, zero out-of-syllabus content, and zero typos. When an authentic past paper originally contained a historical mistake or ambiguity from the examining board (such as UHS or NUMS), BeambePrep faithfully reflects the original paper while detailing the nuance and scientific consensus in the autopsy above.

Want to solve full-length papers under timed exam conditions?

Practice with zero-scroll lockdown sprints, dynamic latency zone timers, live peer selection telemetry, and the automated Amber mistake recovery loop.