1
A reaction consisting of the enolate of a ketone or aldehyde and an alcohol resulting in an hydroxy carbonyl.
2
The process by which one molecule is transformed into another molecule. Could be through enol or enolate intermediates.
3
A reaction where the acid catalyzed elimination of water to result in a t-butyl methyl ketone.
4
When the proton added to the carbon atom with the greatest number of hydrogen atoms attached.
6
A reaction involving two steps, a carbenium ion intermediate, bulky bases, Zaitevs rule, and doesn't require a strong base.
8
A chemical equilibrium between the ketone or aldehyde and an enol (Alcohol).
10
An organic reaction used to convert an alpha,beta unsaturated ketone to an allylic alcohol using cerium trichloride sodium borohydride and an alcohol solvent.
12
What kind of group creates a higher energy intermediate and decreases substitution rate.
13
When the proton added to the carbon atom with the least number of hydrogen atoms attached.
14
An optically active carbonyl compound whose chiral centre is a hydrogen-bearing carbon at the beta position gradually loses its optical activity when its dissolved in an acidic or basic solution.
15
What kind of bases are used for kinetic enolate formation
16
A nucleophilic addition of phenoxide, sodium phenoxide to carbon dioxide resulting in salicylate. After acid workup resulting in salicylic acid.
17
When some Elimination reactions give the least favored and least alkyl-substituted product.
18
An organic reaction used to convert aldehyde or ketone to an alkane using hydrazine, base and thermal conditions.
20
A reaction consisting of a Michael addition and an aldol condensation
21
When a conjugated diene reacts with an alkene at positions 1 and 4 forming a cyclohexene ring.
24
A reaction involving two steps, a secondary/tertiary electrophile, protic polar solvents and has a carbenium ion intermediate.
27
A reaction involving a single step, a primary/secondary electrophile and aprotic polar solvents.