Organic Compounds Containing Nitrogen
Gabriel phthalimide reaction is used for the preparation of:
Why can aromatic primary amines not be prepared by Gabriel phthalimide synthesis?
During Gabriel phthalimide synthesis, the reaction between phthalimide and ethanolic potassium hydroxide gives potassium salt of phthalimide.
The salt on heating with alkyl halide followed by alkaline hydrolysis gives corresponding primary amine.
Aromatic primary amines cannot be prepared by Gabriel phthalimide synthesis as aryl halides do not undergo nucleophilic substitution with the salt formed by phthalimide.
Gabriel phthalimide reaction is used for the preparation of:
Gabriel phthalimide synthesis is used in the preparation of primary amine from phthalimide which of the following reagent is not used during the process?
Which of the following amines can be prepared by Gabriel phthalimide reaction?
Ethylamine $$(C_2H_5NH_2)$$ can be obtained from N-ethylphthalimide on treatment with:
The compound R is:
The compound T is:
Write short note on Gabriel phthalimide synthesis.
Gabriel synthesis is used for the preparation of: a. $$1^{0}$$ amine b. $$2^{0}$$ amine c. $$3^{0}$$ amine d. All can be prepared
The best method for preparing primary amines from alkyl halides without changing the number of carbon atoms in the chain is:
Which of the following amines can be prepared by Gabriel synthesis.