A carbon-carbon bond forming reaction between two esters or an ester and another carbonyl compound in the presence of a strong base.
When a conjugated diene reacts with an alkene at positions 1 and 4 forming a cyclohexene ring.
A reaction involving a single step, a primary/secondary electrophile and aprotic polar solvents.
A reaction involving two steps, a carbenium ion intermediate, bulky bases, Zaitevs rule, and doesn't require a strong base.
A nucleophilic addition of phenoxide, sodium phenoxide to carbon dioxide resulting in salicylate. After acid workup resulting in salicylic acid.
This kind of nucleophile is usually large 3-5th row elements and undergo 1,4 addition.
When the Halide is added to the carbon atom with the greatest number of hydrogen atoms attached.
A reaction consisting of a Michael addition and an aldol condensation
This kind of nucleophile is usually small second row elements and undergo 1,2 addition.
An anion formed when an alpha hydrogen in an aldehyde or ketone is removed
When the Halide is added to the carbon atom with the least number of hydrogen atoms attached.
When some Elimination reactions give the least favored and least alkyl-substituted product.
A reaction involving a single step, no intermediate formation, bulky bases, Zaitevs rule, and require s a strong base.
What kind of bases are used for kinetic enolate formation
What kind of group stabilizes the intermediate and increases substitution rate.
An organic reaction used to convert an alpha,beta unsaturated ketone to an allylic alcohol using cerium trichloride sodium borohydride and an alcohol solvent.
A reaction involving two steps, a secondary/tertiary electrophile, protic polar solvents and has a carbenium ion intermediate.