Advertisements
Advertisements
प्रश्न
Write the main products when methyl chloride is treated with AgCN.
Advertisements
उत्तर
When methyl chloride is treated with AgCN, methyl cyanide is formed.

APPEARS IN
संबंधित प्रश्न
Given reasons: C–Cl bond length in chlorobenzene is shorter than C–Cl bond length in CH3–Cl.
What happens when ethyl chloride is treated with aqueous KOH?
What happens when methyl chloride is treated with KCN?
In the reaction, \[\ce{R - X + NaOR' -> ROR’ + X}\] ( – ve ion). The main product formed is:
Which compound in the following pair reacts faster in SN2 reaction with OH–?
- CH3Br or CH3
- CH3Cl, (CH3)3CCl
Assertion: KCN reacts with methyl chloride to give methyl isocyanide.
Reason: CN– is an ambident nucleophile.
Which of the following statements are correct about this reaction?

(i) The given reaction follows SN2 mechanism.
(ii) (b) and (d) have opposite configuration.
(iii) (b) and (d) have same configuration.
(iv) The given reaction follows SN1 mechanism.
Why are aryl halides less reactive towards nucleophilic substitution reactions than alkyl halides?
Optical activity of an enantiomeric mixture is +12.6° and the specific rotation of (+) isomer is +30°. The optical purity is ______ %.
Give the mechanism of the following reaction:
\[\ce{CH3CH2OH ->[H2SO4][413 K] CH3CH2-O-CH2CH3 + H2O}\]
