Question
Discuss Bischer synthesis of indole. How can you obtain a single product in this reaction?
Answer :
Word Count : 233
Fischer indole synthesis is an important method for the preparation of indole and substituted indoles from aryl hydrazines and aldehydes or ketones under acidic conditions. In this reaction, an aryl hydrazine first reacts with a carbonyl compound to form a hydrazone. On heating with a strong acid such as hydrochloric acid, sulfuric acid, or polyphosphoric acid, the hydrazone ______ __________ _____ ____ ___ _______ ________ ______.
____ ____ _______ _____ __________ __________ ____ __________ ____.
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______.
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Fischer indole synthesis is an important method for the preparation of indole and substituted indoles from aryl hydrazines and aldehydes or ketones under acidic conditions. In this reaction, an aryl hydrazine first reacts with a carbonyl compound to form a hydrazone. On heating with a strong acid such as hydrochloric acid, sulfuric acid, or polyphosphoric acid, the hydrazone ______ __________ _____ ____ ___ _______ ________ ______.
____ ____ _______ _____ __________ __________ ____ __________ ____.
________ ________ ________ ______ _____.
_____ ___ _________ __________ __________ ________.
____ _____ ____ ______ ____ __________ ___ ___.
____ __________ __________ _________ _________ ________.
_____ _______ _____ ___ ________.
_________ _______ _______ ___ __________ ___ ____ ______ ____ ____ _______.
_________ _________ ________ ____ __________ _______ _____ ___ ____ _____.
__________ _________ _______ ___ __________ ________ ________ ___.
_______ ____ _______ ______ ________ ___ __________ __________ ____ _____ ____ _______.
______ ______ ____ ___ __________ _____ _____ ________ _________ _____ ______ _______.
_____ ________ _______ ____ ___ ________ __________ _______.
_________ ____ ____ __________ ___ _____ _____ _______ ___ ____ ________.
__________ _________ _____ _________ ________ ___ ______.
________ ____ _______ ________ ___ ____ ______ __________ _____ ___ _______ _________.
____ ________ _______ __________ _______ ___ ____.
__________ ___ _______ __________ ______ __________ __________ _________ _________.
___ __________ __________ _______ ___ __________ ___ _______ ______.
______ _______ ________ _______ ______ _________ __________ _________ ____ ___ _____.
______.
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