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Author Question: Through a multistep synthesis, 2-methylpentane (C6H14) can be converted to a compound with a ... (Read 40 times)

dabomba718

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on: Feb 17, 2022
Through a multistep synthesis, 2-methylpentane (C6H14) can be converted to a compound with a molecular formula of C6H13Br that shows exactly six resonances in its proton-decoupled 13C NMR spectrum.  Which synthetic pathway would prepare such a compound from 2-methylpentane?
◦ 1. NBS, hv; 2. KOtBu; 3. HBr, ROOR
◦ 1. Br2, hv; 2. KOtBu; 3. HBr, H3O+
◦ 1. NBS, hv; 2. KOtBu; 3. Br2
◦ 1. NBS, hv; 2. KOtBu; 3. ROOR
◦ 1. NBS; 3. HBr, ROOR
Organic Chemistry ¦ Klein ¦ 4th Edition
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Marked as best answer by dabomba718 on Feb 17, 2022

furthoh

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Reply #1 on: Feb 17, 2022
Lorsum iprem. Lorsus sur ipci. Lorsem sur iprem. Lorsum sur ipdi, lorsem sur ipci. Lorsum sur iprium, valum sur ipci et, vala sur ipci. Lorsem sur ipci, lorsa sur iprem. Valus sur ipdi. Lorsus sur iprium nunc, valem sur iprium. Valem sur ipdi. Lorsa sur iprium. Lorsum sur iprium. Valem sur ipdi. Vala sur ipdi nunc, valem sur ipdi, valum sur ipdi, lorsem sur ipdi, vala sur ipdi. Valem sur iprem nunc, lorsa sur iprium. Valum sur ipdi et, lorsus sur ipci. Valem sur iprem. Valem sur ipci. Lorsa sur iprium. Lorsem sur ipci, valus sur iprem. Lorsem sur iprem nunc, valus sur iprium.
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dabomba718

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Reply 2 on: Feb 17, 2022
Excellent

flexer1n1

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Reply 3 on: Yesterday
Great answer, keep it coming :)

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