Question

CНз NBS, CCI4, hv lintermediate product(s) Hас Give all resonance structures of the allylic radical intermediate that arise from reaction above. 2. All allylic C-H on the molecule are equivalent so only show the two resonance structures arising from one C-H bond reacting. 3. Are the resonance structures above equivalent or non-equivalent? Think about the degree of the atom where the radical (the dot) is. Give all the products expected from the reaction above. 4.

Answer 1

The answer is given as follows

- ackence Chalamutic pauce in IR specta for veze a strong at 1600cm Userna medium at 3000-3100 cm Henco concet option is s Ams: - step-I Intermediate formation Bromine (free Radical resun Chat + HO Radica Radicas Abstrachan Ally Radical (2) Resoning stoverture glic radical Ho CH2 IH 4 CH2 HH (I) - CHE of Allister I and I I are are resoning Stonature reson Both I and free radical I and i are has different number (3) Bolh resoning structure non-epnovalet because bol es scalata wil-Hydrogen CamScanner

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