(a) Rate =k [Alkyl Halide][Base] (b) Process follows inversion in stereochemistry (c) Rate of reactivity follows the trend CH3>1°> 2° >3 (d) Mechanism involves carbocations

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Chapter1: Chemical Foundations
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Label the following as: SN1, SN2, E1, E2 reactions. Create examples with drawn mechanisms. 

(a) Rate =k [Alkyl Halide][Base]
(b) Process follows inversion in stereochemistry
(c) Rate of reactivity follows the trend CH3>1°> 2° >3
(d) Mechanism involves carbocations
Transcribed Image Text:(a) Rate =k [Alkyl Halide][Base] (b) Process follows inversion in stereochemistry (c) Rate of reactivity follows the trend CH3>1°> 2° >3 (d) Mechanism involves carbocations
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