imidazolide

Q: Draw the stavetre of ihe following tlave isomeie sanides with chemical forumla CHNO. Amide N1:…

A: Given: The name of the compound is (E)-N,N-dimethyl-2-butenamide. The molecular formula of the…

Q: Explain why carboxylic acids do not undergo nucleophilic acyl substitution reactions with amines.

A: A chemical species which has high electron density or a lone pair of electrons, by using which it…

Q: Which amines cannot be prepared by a Gabriel synthesis? Explain your choices. NH2 NH2 NH2 а. b. C.…

A: Gabriel's phthalimide synthesis is used for the conversion of primary alkyl halide into primary…

Q: What is the major Hofmann elimination product formed from each amine?

A: a. The quaternary amine for the given amine is,

Q: Explain why a secondary amine forms a nitrosamine rather than a diazonium salt when it reacts with…

A:

Q: In the 1880's, Acetanilide, sold under the name Antifebrin, was widely used as a pain reliever and…

A: Here we have to write the mechanism of acid catalyzed hydrolysis of acetanilide and synthesis of…

Q: Explain why a secondary amine forms a nitrosamine rather than a diazonium ion when it reacts with…

A: To understand the reaction consider the reaction of a primary amine with nitrosonium ion. The…

Q: What products are formed when all of the amide and ester bonds are hydrolyzed in each of the…

A: (a) The product formed when all of the amide and ester bonds are hydrolyzed in Oseltamivir of can be…

Q: What products are formed when all of the amide and ester bonds are hydrolyzed in each of the…

A: Hydrolysis refers to cleavage of a bond using water. Amide bond is hydrolysed to give an amine and…

Q: Explain

A: Since you have asked multiple question, we will solve the first question for you.If you want any…

Q: Explain why a secondary amine forms a nitrosamine rather than a diazonium ion when it reacts with a…

A: Given reaction is:

Q: Account for the experimental behavior of each class of amines (primary, secondary and tertiary)…

A: A question based on organic chemistry, which is to be accomplished.

Q: What products are formed when all of the amide and ester bonds arehydrolyzed in each of the…

A: Given compounds: a)oseltamivir b)aspartame

Q: Explain why imidazolides are much more reactive than other amides in nucleophilic acyl substitution.

A: It is known that, imidazolides are much more reactive than other amides in nucleophilic acyl…

Q: Excess ammonia must be used when a primary amine is synthesized by reductive amination. What product…

A: Synthesis of primary amine by reductive elimination takes place as follows:

Q: How imines and enamines are converted back to carbonyl compounds by hydrolysis with mild acid ?

A: Treatment of imines with water leads to their hydrolysis back to aldehydes (or ketones) and an…

Q: In the mid-1930s a substance was isolated from a fungus that is a parasite of ryes and other…

A: Given that, lysergic acid diethylamide (LCD, C20H25N3O). It is a weak base, having Kb = 7.6×10-7.…

Q: Carbonyl compounds can be protonated on the carbonyl oxygen. Protonation of the carbonyl oxygen…

A: Given: Carbonyl compounds can be protonated on the carbonyl oxygen.  Protonation of the carbonyl…

Q: Why is the amine N atom more nucleophilic than the amide N atom in CH3CONHCH2CH2CH2NHCH3?

A: Nucleophilicity of a chemical species depends on availability of electrons on it.  Factors such as…

Q: Compare the physical properties of acid derivatives, and explain the unusually highboiling points…

A: The carboxylic acid and its derivatives have higher boiling point and melting point than the…