Does the Carboxylic acid of tyrosine get deprotonated by NaH? If
so, why is it not...
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Chemistry
Does the Carboxylic acid of tyrosine get deprotonated by NaH? Ifso, why is it not alkylated by the alkyl halide? Comment onnucleophilic strength, and again use structures to explain youranswer Alkyl halide is EtBr
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Yes the carboxylic acid of tyrosine gets easily deprotonated byNaHTo answer the second part of the question it is important tomention that there are two types of sustitution in organicchemistry According to the solvent nucleophile
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