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junior college 1 | H2 Maths
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hi can you help me with qn 4c thanks
Date Posted: 3 years ago
Views: 840
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Top: cis-hex-3-ene
Bottom: trans-hex-3-ene
The 2 isomers react with Br- nucleophile using SN2 nucleophilic substitution mechanism as the carbocation (C with + charge) is surrounded by bulky hydrocarbon groups, leading to steric hindrance.
Since SN2 mechanism is where nucleophile attacks the carbocation from top or bottom of plane *with equal probability*, there are 2 equal proportion of products for each isomer of hex-3-ene.
Let me know if you need further clarification!
Bottom: trans-hex-3-ene
The 2 isomers react with Br- nucleophile using SN2 nucleophilic substitution mechanism as the carbocation (C with + charge) is surrounded by bulky hydrocarbon groups, leading to steric hindrance.
Since SN2 mechanism is where nucleophile attacks the carbocation from top or bottom of plane *with equal probability*, there are 2 equal proportion of products for each isomer of hex-3-ene.
Let me know if you need further clarification!
Date Posted:
3 years ago
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