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Provide three examples (both structure and name for each case) for the following carboxylic acid and...
он он te Acetyl adenosyl phosphate A sum Table 21.1. nclature rules for carboxylic acid derivativ...
он он te Acetyl adenosyl phosphate A sum Table 21.1. nclature rules for carboxylic acid derivatives is given in able 21.1 Nomenclature of Carboxylic Acid Derivatives Functional group Structure Name ending -ic acid (-carboxylic acid) Carboxylic acid -oyl halide (-carbonyl halide) 0 Acid halide anhydride Acid anhydride -amide (-carboxamide Amide -oate (-carboxylate) Ester RT 、NH2 (NHR, NR2) -thioate (-carbothioate) Thioester -oyl phosphate 0 Acyl phosphate 3.) List the functional groups shown in table 21.1 on page 817 in order of...
Which of the following carboxylic acid derivatives is the least reactive in a hydrolysis reaction? Amide...
Which of the following carboxylic acid derivatives is the least reactive in a hydrolysis reaction? Amide Anhydride Ester Acid halide
1) 2) Name each of the following aldehydes and ketones. 3) 4) A carboxylic acid reacts...
1)
2)
Name each of the following aldehydes and ketones.
3)
4)
A carboxylic acid reacts an alcohol to form ________.
an ether
an amine
an anhydride
an ester
an amide
5)
A carboxylic acid reacts with itself to form ________.
an amine
an ether
an anhydride
an ester
an amide
6)
7)
8)
Give the organic product for the following reaction.
CH3CH2COOH + CH3CH2CH2NH2 ?
CH3CH2CH2CONHCH2CH3
CH3CH2NHCH2CH2CH3
CH3CH2N(CH2CH2CH3)2
CH3CH2CON(CH2CH2CH3)2
CH3CH2CONHCH2CH2CH3
Determine the products of the following reaction: CH H2S04...
What is the correct name for the following compound? d) 5-oxo-3-octenoic acid What is the defining...
What is the correct name for the following compound? d) 5-oxo-3-octenoic acid What is the defining functional group of a carboxylic acid? a) an-H attached to a carbonyl group b) an-H attached to a carbon-carbon triple bond c) an-OH attached to a carbonyl group d) an -OH group attached to a O-C double bond e) an-OH group attached to an aromatic ring To convert a carboxylic acid to an aldehyde a) convert the acid to an acid chloride, then use...
a cari b. acid chloride c. ester For each of the terms on the left, provide...
a cari b. acid chloride c. ester For each of the terms on the left, provide the best match from the choices on the right. (each choice is only used once). (2@) 1. hydrazone 2. NaBH 3. lithium dialkylcuprate 4. Haloform reaction 5. hydrazone 6. Li[(-Bu0);AIH] 7. Trans-esterification 8. Silyl ether 9. Concerted Reaction 10. BH; 11. Arenium ion 12. acetal 13. Wolff-Kishner 14. Acyl substitution 15. DIBAL-H __16. Sandmeyer Reaction _17. Diazotization _18. Wittig Reaction 19. Claisen Condensation 20....
b. acid chloride c. ester For each of the terms on the left, provide the best...
b. acid chloride c. ester For each of the terms on the left, provide the best match from the choices on the right. (each choice is only used once). (2@) 1. hydrazone 2. NaBH4 3. lithium dialkylcuprate 4. Haloform reaction 5. hydrazone 6. Li[(t-Bu0)AIH] 7. Trans-esterification 8. Silyl ether 9. Concerted Reaction 10. BH; 11. Arenium ion 12. acetal 13. Wolff-Kishner 14. Acyl substitution 15. DIBAL-H 16. Sandmeyer Reaction 17. Diazotization 18. Wittig Reaction 19. Claisen Condensation __20. Baeyer-Villiger A....
POST-LABORATORY EXERCISES mic Acid Oxidation of Cyclohexanol Chromic Acid Oxid 1. Suppose instead of ead of...
POST-LABORATORY EXERCISES mic Acid Oxidation of Cyclohexanol Chromic Acid Oxid 1. Suppose instead of ead of using chromic acid as the oxidizing agent, you wed concentrated sulfuric acid. em to show the oxidation of cyclohexanol to cyclohexanone. W 1. Waite a mechanism to show the oxidatinast 개 wi 2. How would you carry out the following transformation? GENERAL EXPERIMENTAL ORGANIC CHEMIST action (If it has a name) and 3. Some of the reactions below are write the products of each...
Can someone help with the 4 POST LAB questions thanks Carboxylic Acids and Esters acid). like...
Can someone help with the 4 POST LAB questions thanks
Carboxylic Acids and Esters acid). like citric acid. Face crearboxyl the name implies, a Carbexylic Aclds A salad dressing made of The sour taste of fruits such as lemons is due to the presence of acids like citric acid. tcarboxyl a-hydroxy acids such functional group - that is, a carbonyl group attached to a hydroxyl group. AS dicarboxylic acid carboxylic acid of benzene is called benzoic acid (Figure 1). oil...
1) Name the following carboxylic acids (use both IUPAC and common names): ОН ОН (b) (c)...
1) Name the following carboxylic acids (use both IUPAC and common names): ОН ОН (b) (c) ОН ОН (d) Br ОН ОН NH2 2) Draw the condensed and line structures for the following compounds (a) 3,4-dimethylhexanoic acid (b) Phenylacetic acid (c) 3,4-dinitrobenzoic acid (d) 2,2,3-triflurobutanoic acid (e) 3-hydroxybutanoic acid (1) o-hydroxybenzoic acid (g) a-aminopropionic acid 3) Name the following dicarboxylic acids (use both IUPAC and common names) Он (а) НО ОН НО. (b) он ОН ОН (d) ОН он ОН...
1. Matching. For each functional group on the left, select the reducing agent(s) on the right...
1. Matching. For each functional group on the left, select the reducing agent(s) on the right that WILL successfully react with the given functional group. Write the letter that corresponds to the correct answer on the line next to the functional group. once, and you may or may not use all of the possible answers. (5 pts) You will use one or more of the answers more than carboxylic acid a) LiAIH b) NaBH c) both LiAlH4 and NaBH4 d)...
он он te Acetyl adenosyl phosphate A sum Table 21.1. nclature rules for carboxylic acid derivatives is given in able 21.1 Nomenclature of Carboxylic Acid Derivatives Functional group Structure Name ending -ic acid (-carboxylic acid) Carboxylic acid -oyl halide (-carbonyl halide) 0 Acid halide anhydride Acid anhydride -amide (-carboxamide Amide -oate (-carboxylate) Ester RT 、NH2 (NHR, NR2) -thioate (-carbothioate) Thioester -oyl phosphate 0 Acyl phosphate 3.) List the functional groups shown in table 21.1 on page 817 in order of...
Which of the following carboxylic acid derivatives is the least reactive in a hydrolysis reaction? Amide Anhydride Ester Acid halide
1)
2)
Name each of the following aldehydes and ketones.
3)
4)
A carboxylic acid reacts an alcohol to form ________.
an ether
an amine
an anhydride
an ester
an amide
5)
A carboxylic acid reacts with itself to form ________.
an amine
an ether
an anhydride
an ester
an amide
6)
7)
8)
Give the organic product for the following reaction.
CH3CH2COOH + CH3CH2CH2NH2 ?
CH3CH2CH2CONHCH2CH3
CH3CH2NHCH2CH2CH3
CH3CH2N(CH2CH2CH3)2
CH3CH2CON(CH2CH2CH3)2
CH3CH2CONHCH2CH2CH3
Determine the products of the following reaction: CH H2S04...
What is the correct name for the following compound? d) 5-oxo-3-octenoic acid What is the defining functional group of a carboxylic acid? a) an-H attached to a carbonyl group b) an-H attached to a carbon-carbon triple bond c) an-OH attached to a carbonyl group d) an -OH group attached to a O-C double bond e) an-OH group attached to an aromatic ring To convert a carboxylic acid to an aldehyde a) convert the acid to an acid chloride, then use...
a cari b. acid chloride c. ester For each of the terms on the left, provide the best match from the choices on the right. (each choice is only used once). (2@) 1. hydrazone 2. NaBH 3. lithium dialkylcuprate 4. Haloform reaction 5. hydrazone 6. Li[(-Bu0);AIH] 7. Trans-esterification 8. Silyl ether 9. Concerted Reaction 10. BH; 11. Arenium ion 12. acetal 13. Wolff-Kishner 14. Acyl substitution 15. DIBAL-H __16. Sandmeyer Reaction _17. Diazotization _18. Wittig Reaction 19. Claisen Condensation 20....
b. acid chloride c. ester For each of the terms on the left, provide the best match from the choices on the right. (each choice is only used once). (2@) 1. hydrazone 2. NaBH4 3. lithium dialkylcuprate 4. Haloform reaction 5. hydrazone 6. Li[(t-Bu0)AIH] 7. Trans-esterification 8. Silyl ether 9. Concerted Reaction 10. BH; 11. Arenium ion 12. acetal 13. Wolff-Kishner 14. Acyl substitution 15. DIBAL-H 16. Sandmeyer Reaction 17. Diazotization 18. Wittig Reaction 19. Claisen Condensation __20. Baeyer-Villiger A....
POST-LABORATORY EXERCISES mic Acid Oxidation of Cyclohexanol Chromic Acid Oxid 1. Suppose instead of ead of using chromic acid as the oxidizing agent, you wed concentrated sulfuric acid. em to show the oxidation of cyclohexanol to cyclohexanone. W 1. Waite a mechanism to show the oxidatinast 개 wi 2. How would you carry out the following transformation? GENERAL EXPERIMENTAL ORGANIC CHEMIST action (If it has a name) and 3. Some of the reactions below are write the products of each...
Can someone help with the 4 POST LAB questions thanks
Carboxylic Acids and Esters acid). like citric acid. Face crearboxyl the name implies, a Carbexylic Aclds A salad dressing made of The sour taste of fruits such as lemons is due to the presence of acids like citric acid. tcarboxyl a-hydroxy acids such functional group - that is, a carbonyl group attached to a hydroxyl group. AS dicarboxylic acid carboxylic acid of benzene is called benzoic acid (Figure 1). oil...
1) Name the following carboxylic acids (use both IUPAC and common names): ОН ОН (b) (c) ОН ОН (d) Br ОН ОН NH2 2) Draw the condensed and line structures for the following compounds (a) 3,4-dimethylhexanoic acid (b) Phenylacetic acid (c) 3,4-dinitrobenzoic acid (d) 2,2,3-triflurobutanoic acid (e) 3-hydroxybutanoic acid (1) o-hydroxybenzoic acid (g) a-aminopropionic acid 3) Name the following dicarboxylic acids (use both IUPAC and common names) Он (а) НО ОН НО. (b) он ОН ОН (d) ОН он ОН...
1. Matching. For each functional group on the left, select the reducing agent(s) on the right that WILL successfully react with the given functional group. Write the letter that corresponds to the correct answer on the line next to the functional group. once, and you may or may not use all of the possible answers. (5 pts) You will use one or more of the answers more than carboxylic acid a) LiAIH b) NaBH c) both LiAlH4 and NaBH4 d)...
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