Which of the following strategies is NOT expected to effect the reduction of 4-tert-butanol to tert-butylcyclohexane.ReactionconditionsO LIAIH4, THFO NH2NH2, KOHO Zn(Hg), HCIO HSCH2CH2SH, H*; ) H2, Raney Ni°

->Carbonyl compound reduce to alcohol when reacts with reducing agent LiAlH4,THF.

Which of the tollowing strategies is NOT expected to effect the reduction of 4-tert-butanol to tert-butylcy Reaction conditions O LIAIH4. THF O NH2NH2, KOH O Zn(Hg), HCI OHSCH2CH2SH, H*, i) H2 Raney Ni

Which of the tollowing strategies is NOT expected to effect the reduction of 4-tert-butanol to tert-butylcy Reaction conditions O LIAIH4. THF O NH2NH2, KOH O Zn(Hg), HCI OHSCH2CH2SH, H*, i) H2 Raney Ni

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter16: Chemistry Of Benzene: Electrophilic Aromatic Substitution

Section16.SE: Something Extra

Problem 30MP: The carbocation electrophile in a Friede1-Crafts reaction can be generated by an alternate means...

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Designing a Synthesis

Organic synthesis is a branch of chemical synthesis that involves the planned construction of organic compounds/molecules from smaller units that possess functional groups. Friedrich Wöhler was the first scientist who designed the synthesis of an organic compound, urea from inorganic starting materials silver cyanate with ammonium chloride via a simple, one-step synthesis.

Question

Which of the following strategies is NOT expected to effect the reduction of 4-tert-butanol to tert-butylcyclohexane.
Reaction
conditions
O LIAIH4, THF
O NH2NH2, KOH
O Zn(Hg), HCI
O HSCH2CH2SH, H*; ) H2, Raney Ni°

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