front 1 Ester formation from carboxylic acid Product: Reagent: | back 1 no data |
front 2 Carboxylic acid + hydroxy group form cyclic esters Product: Reagent: | back 2 no data |
front 3 Formation of acid chlorides from carboxylic acid Product: Reagent: | back 3 no data |
front 4 Amides/Ester formation from acid chlorides Product: Reagent: | back 4 no data |
front 5 Ester/Amide formation from cyclic anhydrides Product: Reagent: | back 5 no data |
front 6 Methyl ester formation from carboxylic acids Product: Reagent: | back 6 no data |
front 7 Amide formation from ester/amines Product: Reagent: | back 7 no data |
front 8 Ester hydrolysis to carboxylic acid Product: Reagent: | back 8 no data |
front 9 Saponification Product: Reagent: | back 9 no data |
front 10 Amide hydroysis of Acid Product: Reagent: | back 10 no data |
front 11 Amide hydrolysis of Base Product: Base: | back 11 no data |
front 12 Amide formation from nitriles Product: Reagent: | back 12 no data |
front 13 Nitrile hydrolysis of acid Product: Reagent: | back 13 no data |
front 14 Nitrile hydrolysis of base Product: | back 14 no data |
front 15 Ketone formation from acid chloride Product: Reagent: | back 15 no data |
front 16 Tertiary alcohol formation from esters Product: Reagent: | back 16 no data |
front 17 Carboxylic acids and esters are reduced to form primary alcohols Product: Reagent: | back 17 no data |
front 18 Reduction of amides to form amines Product: Reagent: | back 18 no data |
front 19 Aldehyde formation from acid chlorides Product: Reagent: | back 19 no data |