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А Treatment of (S)-(+)-5-methyl-2-cyclohexenone with lithium dimethylcuprate gives, after protonolysis, a good yield of a mixture...
Trearment of (S)-(+)-5methylcyclohex-2-enone with lithium dimethlycuprate gives, after protonolysis, a good yield of a mixture containing...
Trearment of
(S)-(+)-5methylcyclohex-2-enone with lithium dimethlycuprate gives,
after protonolysis, a good yield of a mixture containing mostly
dextrorotary Ketone A and a trace of optically inactive isomer B.
Treatment of A with zinc amalgam and HCl affords opticlly active
hydrocarbon C (C8H16). Compound B, which exhibits only 5 unique
signals in its 13C NMR spectrum, undergoes an aldol condensation
with NaOEt and benzaldehyde to produce optically active compound D.
Identify componds A-Dincluding stereochemical configurations.
Treatment of (S)- (+-5-methylcyclohex-2-enone with lithium...
Trearment of
(S)-(+)-5methylcyclohex-2-enone with lithium dimethlycuprate gives,
after protonolysis, a good yield of a mixture containing mostly
dextrorotary Ketone A and a trace of optically inactive isomer B.
Treatment of A with zinc amalgam and HCl affords opticlly active
hydrocarbon C (C8H16). Compound B, which exhibits only 5 unique
signals in its 13C NMR spectrum, undergoes an aldol condensation
with NaOEt and benzaldehyde to produce optically active compound D.
Identify componds A-Dincluding stereochemical configurations.
Treatment of (S)- (+-5-methylcyclohex-2-enone with lithium...
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