10. Please show how each compound might be synthesized by the Sx2 displacement of an alkyl halide. (Hint: Find a proper nucleophile and a suitable alkyl halde.) (a) (b) 'tor (c)

Organic Chemistry
9th Edition
ISBN:9781305080485
Author:John E. McMurry
Publisher:John E. McMurry
Chapter5: Stereochemistry At Tetrahedral Centers
Section5.SE: Something Extra
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10. Please show how each compound might be synthesized by the SN2 displacement of an alkyl
halide. (Hint: Find a proper nucleophile and a suitable alkyl halde.)
(а)
(b)
(c)
(d)
(e)
Transcribed Image Text:10. Please show how each compound might be synthesized by the SN2 displacement of an alkyl halide. (Hint: Find a proper nucleophile and a suitable alkyl halde.) (а) (b) (c) (d) (e)
3.
Two substitution products result from the reaction of 3-chloro-3-methyl-1-butene with
sodium acetate (CH:CO2 Na*) in acetic acid under SN1 conditions. Identify the products.
(Hint: Resonance form)
Please predict the products in the following reactions. (Hint: Stereochemistry!!)
CH,CH3
SN2 conditions
+ НО-
CH3 Br
(S)-2-bromobutane
CH,CH3
SN1 conditions
+ H,O
CH3 Br
(S)-2-bromobutane
4.
Transcribed Image Text:3. Two substitution products result from the reaction of 3-chloro-3-methyl-1-butene with sodium acetate (CH:CO2 Na*) in acetic acid under SN1 conditions. Identify the products. (Hint: Resonance form) Please predict the products in the following reactions. (Hint: Stereochemistry!!) CH,CH3 SN2 conditions + НО- CH3 Br (S)-2-bromobutane CH,CH3 SN1 conditions + H,O CH3 Br (S)-2-bromobutane 4.
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