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Carboxylic Acid Derivatives (21) 1. Nomenclatures For each of the compounds shown below, provide an acceptable...
Gonna G Name FUNCTIONAL GROUPS Classify each of the organic compounds below as an alcohol, carboxylic acid, aldehyd...
Gonna G Name FUNCTIONAL GROUPS Classify each of the organic compounds below as an alcohol, carboxylic acid, aldehyde. ketone, ether or ester, and draw its structural formula Cafeamgc H-C-C-OH 6. сHсконсн, 1. CH,COOH acid 2. CH,COCH, 7. сHсHсOон 3. CH,CH,OH 8. СнсHсоосH, 9. CH,CH,COCH, 4. CH,CH,OCH, 10. CH,OCH 5. CH,CH,CHO
Gonna G Name FUNCTIONAL GROUPS Classify each of the organic compounds below as an alcohol, carboxylic acid, aldehyde. ketone, ether or ester, and draw its structural formula Cafeamgc H-C-C-OH 6....
page 2 Chem 102 Work Shot 9.0 Dr.O. Amino Acids NAME_Sheena Thompson For each amino acid:...
page 2 Chem 102 Work Shot 9.0 Dr.O. Amino Acids NAME_Sheena Thompson For each amino acid: A. Draw a circle around the carboxylic acid group B. Drow a triangle around the c-amino group C. Draw a box (or rectangle or polygon) around the Rgroup in each amino acid D. Use hi-lighters or colored pencils on each name to classify the amino acids as one of the following: 1. Nonpolar 2. Polar neutral 3. Polar acidic 4. Polor basic NH CO_H...
Amides are prepared from carboxylic acid derivatives. In the reaction shown below, what is the correct...
Amides are prepared from carboxylic acid derivatives. In the reaction shown below, what is the correct structure for the missing reactant? Cheryl CH3CH2C-CI + 2(?) - CH₃CHY & N-CH3 + by-product CH3CH2C-N-CH3 CH2CH3 main product H H-N-CH2CH3 (A) CH2CH3 H-N-CH3 (B) CH2CH3 H-N-CH2CH3 (C) CH3 H-N-CH3 (D) Select one: O (A) (B) (C) (D) None of these
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...
Please answer all questions. Chapter 21, Practice problems (Carboxylic Acid Derivatives) 1) Amides are less basic...
Please answer all questions.
Chapter 21, Practice problems (Carboxylic Acid Derivatives) 1) Amides are less basic than amines because A) the carbonyl group donates electrons by resonance B) the carbonyl group withdraws electrons by resonance C) the nitrogen does not have a lone pair of electrons D) the nitrogen has a full positive charge E) amides do not contain nitrogen 2) N-Methylacetamide is an example of A) a primary amide B) a secondary amide C) a tertiary amide D) an...
General Module 1. Identify the fumily of each of the following compounds b) CH, CH,O CH,...
General Module 1. Identify the fumily of each of the following compounds b) CH, CH,O CH, CH, CH, 2. Write siructural formulas for the following compounds: s a) 3-chloro-2-methylheptanal @ d) 3-methyl-4-hexene-2-ol II-H cz 3. Which of the following are nonsaponifiable lipids? i) waxes j) leukotrienes k) plasmalogens a) triacylglycerols b) oils c) sphingomyelins d) steroids c) terpenes f)" sphyngolipids g) glycolipids h) prostoglandins 4. Write the equation showing triacylglycerol from glycerol and oleic, palmitic and stearic acids 5. Point...
1. (48 pts, 4 pts each) Give an acceptable IUPAC name for the following compound: CH)...
1. (48 pts, 4 pts each) Give an acceptable IUPAC name for the following compound: CH) i 0 CO,H CH, OH Font Font COOH CH,_ch, bi-ch, bi-CH, CN CH OH CHO Font соон NO 2. (36 pts, 4 pts each) Draw a structure for the following compounds: a. 2-Amino-2-methylbutanol b. 4-Hexynol C. 3-Methoxycycloheptanecarboxylic acid d. 2-Phenylethanol e. 3-Hydroxycyclopentanecarboxamide f. 4-Bromobenzaldehyde Font g. 6-Bromohexanoic acid h. 2, 3, 4-Hexanetriol L1-Decanthi 3. (16 pts, 4 pts each) Draw a structural formula for...
practice complely the follow, + NaOH following (Fill in the Blanks (ose wnds carboxylic Acid +...
practice
complely the follow, + NaOH following (Fill in the Blanks (ose wnds carboxylic Acid + Amine water carboxylic Aad & Alcohol Carboxylic Acid water Esten + H₂O + tre hydrolysis? Amide + H₂O titre hydedlysis Show the reagent / reagents needed to make the following molecolar conversions. Show reagent (s) to the right. Seach=40 HC=CH₂ HC-CH₃ 4 ة= SH please note: the is an aromated ring. It does not atlect the chemistry Hocao 0 ÖzçēH (oxidation? bacco in there...
please help me identify each numbered peak beyond 1500 cm-1. For each peak above 3000 cm-1...
please help me identify each numbered peak beyond 1500 cm-1.
For each peak above 3000 cm-1 please identify them as sp1, sp2 or
sp3.
* * 3 * B&BRE 400 000 000 200 00 00 Pure Ethanol 2023.83 DOKOMOKO OZ REKON O em G 00 200 000 6 Unknown A853 0 0 1438.63 WhO Unknown 200 KED B297 RO 107.17 FON: 2000 2000 2000 2100 2200 2000 1200 900 900 WOO 200 000 ethanol Intensity of Signal How to The...
____ 1. The diagram below represents serine, a polar, uncharged amino acid. Which functional group gives...
____ 1. The diagram below represents serine, a polar, uncharged
amino acid. Which functional group gives serine its
distinct property?
a. H3
b. CH2OH
c. –H
d. COO–
____ 2. The monomers shown below are monomers for which of the
following natural polymers?
a. polysaccharides
b. plastics
c. DNA
d. proteins
____ 3. Which of the following processes illustrates the production
of a protein?
a. specific code for amino acids --> amino acid chain -->
gene --> DNA --> specific...
Gonna G Name FUNCTIONAL GROUPS Classify each of the organic compounds below as an alcohol, carboxylic acid, aldehyde. ketone, ether or ester, and draw its structural formula Cafeamgc H-C-C-OH 6. сHсконсн, 1. CH,COOH acid 2. CH,COCH, 7. сHсHсOон 3. CH,CH,OH 8. СнсHсоосH, 9. CH,CH,COCH, 4. CH,CH,OCH, 10. CH,OCH 5. CH,CH,CHO
Gonna G Name FUNCTIONAL GROUPS Classify each of the organic compounds below as an alcohol, carboxylic acid, aldehyde. ketone, ether or ester, and draw its structural formula Cafeamgc H-C-C-OH 6....
page 2 Chem 102 Work Shot 9.0 Dr.O. Amino Acids NAME_Sheena Thompson For each amino acid: A. Draw a circle around the carboxylic acid group B. Drow a triangle around the c-amino group C. Draw a box (or rectangle or polygon) around the Rgroup in each amino acid D. Use hi-lighters or colored pencils on each name to classify the amino acids as one of the following: 1. Nonpolar 2. Polar neutral 3. Polar acidic 4. Polor basic NH CO_H...
Amides are prepared from carboxylic acid derivatives. In the reaction shown below, what is the correct structure for the missing reactant? Cheryl CH3CH2C-CI + 2(?) - CH₃CHY & N-CH3 + by-product CH3CH2C-N-CH3 CH2CH3 main product H H-N-CH2CH3 (A) CH2CH3 H-N-CH3 (B) CH2CH3 H-N-CH2CH3 (C) CH3 H-N-CH3 (D) Select one: O (A) (B) (C) (D) None of these
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...
Please answer all questions.
Chapter 21, Practice problems (Carboxylic Acid Derivatives) 1) Amides are less basic than amines because A) the carbonyl group donates electrons by resonance B) the carbonyl group withdraws electrons by resonance C) the nitrogen does not have a lone pair of electrons D) the nitrogen has a full positive charge E) amides do not contain nitrogen 2) N-Methylacetamide is an example of A) a primary amide B) a secondary amide C) a tertiary amide D) an...
General Module 1. Identify the fumily of each of the following compounds b) CH, CH,O CH, CH, CH, 2. Write siructural formulas for the following compounds: s a) 3-chloro-2-methylheptanal @ d) 3-methyl-4-hexene-2-ol II-H cz 3. Which of the following are nonsaponifiable lipids? i) waxes j) leukotrienes k) plasmalogens a) triacylglycerols b) oils c) sphingomyelins d) steroids c) terpenes f)" sphyngolipids g) glycolipids h) prostoglandins 4. Write the equation showing triacylglycerol from glycerol and oleic, palmitic and stearic acids 5. Point...
1. (48 pts, 4 pts each) Give an acceptable IUPAC name for the following compound: CH) i 0 CO,H CH, OH Font Font COOH CH,_ch, bi-ch, bi-CH, CN CH OH CHO Font соон NO 2. (36 pts, 4 pts each) Draw a structure for the following compounds: a. 2-Amino-2-methylbutanol b. 4-Hexynol C. 3-Methoxycycloheptanecarboxylic acid d. 2-Phenylethanol e. 3-Hydroxycyclopentanecarboxamide f. 4-Bromobenzaldehyde Font g. 6-Bromohexanoic acid h. 2, 3, 4-Hexanetriol L1-Decanthi 3. (16 pts, 4 pts each) Draw a structural formula for...
practice
complely the follow, + NaOH following (Fill in the Blanks (ose wnds carboxylic Acid + Amine water carboxylic Aad & Alcohol Carboxylic Acid water Esten + H₂O + tre hydrolysis? Amide + H₂O titre hydedlysis Show the reagent / reagents needed to make the following molecolar conversions. Show reagent (s) to the right. Seach=40 HC=CH₂ HC-CH₃ 4 ة= SH please note: the is an aromated ring. It does not atlect the chemistry Hocao 0 ÖzçēH (oxidation? bacco in there...
please help me identify each numbered peak beyond 1500 cm-1.
For each peak above 3000 cm-1 please identify them as sp1, sp2 or
sp3.
* * 3 * B&BRE 400 000 000 200 00 00 Pure Ethanol 2023.83 DOKOMOKO OZ REKON O em G 00 200 000 6 Unknown A853 0 0 1438.63 WhO Unknown 200 KED B297 RO 107.17 FON: 2000 2000 2000 2100 2200 2000 1200 900 900 WOO 200 000 ethanol Intensity of Signal How to The...
____ 1. The diagram below represents serine, a polar, uncharged
amino acid. Which functional group gives serine its
distinct property?
a. H3
b. CH2OH
c. –H
d. COO–
____ 2. The monomers shown below are monomers for which of the
following natural polymers?
a. polysaccharides
b. plastics
c. DNA
d. proteins
____ 3. Which of the following processes illustrates the production
of a protein?
a. specific code for amino acids --> amino acid chain -->
gene --> DNA --> specific...
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