Gabriel Synthesis is a chemical reaction that is responsible for the conversion of alkyl halides (haloalkanes) into primary amines. This reaction commonly uses potassium phthalimide as a reagent in it. In this reaction, the sulfonamides and imides are first alkylated and then are deprotonated.
In this way, the amines are obtained. Ammonia is not a suitable route to amines, hence phthalimide anion is used as a substitute for H2 N -. Other reagents such as sodium salt of saccharin and di-tert-butyl-iminodicarboxylate can act on secondary haloalkanes and hydrolyze them more easily resultantly from secondary amines.
Draw a mechanism for each of the following transformations: /
Draw and name four terminal alkynes with the molecular formula C6H10.
Propose a stepwise mechanism for the following transformation: /
Write an equation for the proton transfer reaction that occurs when each
Identify the sole product of the following reaction: /
Firefly luciferin is the compound that enables fireflies to glow.
Scorzocreticin (S)-1 was isolated from a plant that is
Draw the condensation product that is expected when each of the following
87. What is the major product of this reaction?
Report the result of the following addition to the proper number of
