Chemistry - Halogen Derivative Question with Solution | TestHub

ChemistryHalogen DerivativeMiscellaneous/MixedEasy2 minPYQ_2020
ChemistryEasynumerical

How many of the statement(s) are correct
i) The nucleophile makes a rear attack in S N 2 reaction and expels the leaving group from front side.
ii)CH3O-CH=CH2adds to HBr according to Anti‐Markownikoff’s rule.
iii) The basicity of halides decreases in the orderF->C1->Br->I-,but the nucleophillicity is reverse of it. (in polar protic solvents)
iv) The rate of S N 2 reaction is independent of the polarity of the solvent.
v) Sigma complex or arenium ion is resonance stablised.

Answer:
3.00
Solution:

i) The nucleophile makes a rear attack in S N 2 reaction and expels the leaving group from front side.
iii) The basicity of halides decreases in the orderF->C1->Br->I-,but the nucleophillicity is reverse of it. (in polar protic solvents)
v) Sigma complex or arenium ion is resonance stablised.
The above statements are correct.
CH3O-CH=CH2adds to HBr according to Markownikoff’s rule.
iv) The rate of S N 2 reaction is faster in polar aprotic solvent.

Stream:NTA_ABHYASSubject:ChemistryTopic:Halogen DerivativeSubtopic:Miscellaneous/Mixed
2mℹ️ Source: PYQ_2020

Doubts & Discussion

Loading discussions...