1)
All are tertiary alkyl halides.
The leaving groups in three compounds are Br-, I- and Cl-
Amount these three I- is good leaving group.
Therefore the most reactive compound in an SN1 reaction is II.
2)
H
here the alkyl halide is tertiary so it undergoes SN1 reaction.
The rate of SN1 Reaction is only depends on the concentration of alkyl halide but not on the concentration of nucleophile.
Rate = k[alkyl halide]
If the concentration of alkyl halide and nucleophile is double then rate is,
Rate = k[2× alkyl halide]
Rate = 2 × k[alkly halide]
Hence the rate of reaction is double.
Therefore the correct option is (c) doubles the rate
3)
The reactivity order of alkyl halides towards SN1 reaction is as follows:
3° > 2° > 1° > CH3-X
Compound I is tertiary alkyl halide.
Compound II is secondary alkyl halide
Compound is III is primary alkyl halide.
compound I is most reactive in an SN1 reaction
Therefore the correct option is (I)
Select which compound is the most reactive in an SN1 reaction Br Select one: O III...
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Q1) Which compound will undergo SN1 reaction fastest? CI Cl Q2) What is true about SN1 reaction of alkyl halides? a) Reaction favored by non-polar solvents. b) Reaction rate depends on concentration of alkyl halide c) SN1 proceeds in one step thru transition state d) Reaction rate depends on concentration of nucleophile
Which compound is the most reactive in an Sn1 reaction?
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