Textbook QuestionUsing cyclohexanone as the starting material, describe how each of the following compounds can be synthesized: e. 511views
Textbook QuestionThe compounds commonly known as 'amino acids' are actually α-aminocarboxylic-aminocarboxylic acids (SECTION 21.0 ). What carbonyl compounds should be used to synthesize the two amino acids shown here? b. 476views
Textbook QuestionThe compounds commonly known as 'amino acids' are actually α-aminocarboxylic-aminocarboxylic acids (SECTION 21.0 ). What carbonyl compounds should be used to synthesize the two amino acids shown here? a. 440views
Textbook QuestionExcess ammonia must be used when a primary amine is synthesized by reductive amination. What product will be obtained if the reaction is carried out with excess carbonyl compound?386views
Textbook QuestionThe two most general amine syntheses are the reductive amination of carbonyl compounds and the reduction of amides. Show how these techniques can be used to accomplish the following syntheses. (b) benzaldehyde → benzylamine693views
Textbook QuestionShow how to synthesize the following amines from the indicated starting materials by reductive amination. (a) benzylmethylamine from benzaldehyde (b) N-benzylpiperidine from piperidine (c) N-cyclohexylaniline from cyclohexanone569views
Textbook QuestionUsing cyclohexanone as the starting material, describe how each of the following compounds can be synthesized:d. <IMAGE>271views
Textbook QuestionShow how m-toluidine can be converted tothe following compounds, using any necessary reagents.<IMAGE>(f) <IMAGE>210views
Textbook QuestionUsing any necessary reagents, show how you would accomplish the following syntheses.(d) <IMAGE of reaction>200views
Textbook QuestionShow how you would use the same sulfonyl chloride as used in the sulfanilamide synthesis to make sulfathiazole and sulfapyridine.<IMAGE>206views
Textbook QuestionShow how to synthesize the following amines from the indicated starting materials by reductive amination.(e) <IMAGE>171views
Textbook QuestionShow how you can synthesize the following tertiary amine three different ways, each using a different secondary amine and adding the final substituent by(a) reductive amination (3 ways). <IMAGE>212views
Textbook QuestionShow how you can synthesize the following compounds starting with benzene, toluene, and alcohols containing no more than four carbon atoms as your organic starting materials. Assume that para is the major product (and separable from ortho) in ortho, para mixtures.(c) N-ethyl-N-propylbutan-2-amine212views
Textbook QuestionShow how you can synthesize the following compounds starting with benzene, toluene, and alcohols containing no more than four carbon atoms as your organic starting materials. Assume that para is the major product (and separable from ortho) in ortho, para mixtures.(d) N-benzylpropan-1-amine167views
Textbook QuestionThe two most general amine syntheses are the reductive amination of carbonyl compounds and the reduction of amides. Show how these techniques can be used to accomplish the following syntheses.(d) cyclohexanone → N-cyclohexylpyrrolidine192views
Textbook QuestionWhat would happen in the synthesis of sulfanilamide if the amino group were not protected as an amide in the chlorosulfonation step?203views
07:12
