(a)
Interpretation:
The
Concept introduction:
The reaction between
(b)
Interpretation:
The amine and carbonyl compound that will combine to provide the given derivative are to be stated.
Concept introduction:
The reaction between ketone/aldehyde and ammonia derivatives in mild acidic condition comprises two steps. First is the acid catalyzed addition of the amine to the carbonyl group. Second is acid catalyzed dehydration to get the desired product (an imine).
(c)
Interpretation:
The amine and carbonyl compound that will combine to provide the given derivative are to be stated.
Concept introduction:
The reaction between ketone/aldehyde and ammonia derivatives in mild acidic condition comprises two steps. First is the acid catalyzed addition of the amine to the carbonyl group. Second is acid catalyzed dehydration to get the desired product (an imine).
(d)
Interpretation:
The amine and carbonyl compound that will combine to provide the given derivative are to be stated.
Concept introduction:
The reaction between ketone/aldehyde and ammonia derivatives in mild acidic condition comprises two steps. First is the acid catalyzed addition of the amine to the carbonyl group. Second is acid catalyzed dehydration to get the desired product (an imine).
(e)
Interpretation:
The amine and carbonyl compound that will combine to provide the given derivative are to be stated.
Concept introduction:
The reaction between ketone/aldehyde and ammonia derivatives in mild acidic condition comprises two steps. First is the acid catalyzed addition of the amine to the carbonyl group. Second is acid catalyzed dehydration to get the desired product (an imine).
(f)
Interpretation:
The amine and carbonyl compound that will combine to provide the given derivative are to be stated.
Concept introduction:
The reaction between ketone/aldehyde and ammonia derivatives in mild acidic condition comprises two steps. First is the acid catalyzed addition of the amine to the carbonyl group. Second is acid catalyzed dehydration to get the desired product (an imine).
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Organic Chemistry (9th Edition)
- Amides can be form by; Group of answer choices oxidation of ether oxidation of aldehydes and ketones reaction of carboxylic acid to alcohol reaction of carboxylic acid to aminearrow_forwardFollowing is an ---- and called ---, respectively. ester, methyl hexanoate ester, methyl butanoate ester, ethyl pentanoate ether, methyl butanoatearrow_forwardThe molecule contains carbon atoms (shown in black), Consider the structure and determine what classes this hydrogen (white), and oxygen (red). compound belongs to. Note: only sigma-bond connectivity is shown, and there are no formal charges. alkyl halide amide O alkyne aromatic/arene acid anhydride thiol ketone alcohol acid chloride carboxylic acid amine ether O aldehyde ester alkenearrow_forward
- Acid Anhydride Amine Thiol Peroxide Nitrile Arenearrow_forwardRank the following functional groups from least to most reactive: acid anhydride, acyl chloride, amide, and ester.arrow_forwardGive the general structures, example, (with structures) and functional group of these type of compounds: Alkyl Halide, Alcohol, Ether, Amine, Aldehyde, Ketone, Carboxylic Acids, Ester, and Amide.arrow_forward
- Why are carbonyl compounds considered weakly acidic? Would you expect carbonyl compounds to be more acidic than alkanes? Explain.arrow_forwardKetone Amine Ester Carboxylic Acid Amide Nitrile Peroxide Alkyne Thiolarrow_forwardDefine Spectroscopic Properties of carboxylic acid derivatives ?arrow_forward
- Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning