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e. E) -CH20H 15. The reaction of butanoic acid and dimethylamine gives a. N-methylbutanamide b. N-ethylbutanamide...
HO CH сн. CH2 нс HC CH3 HAC-HC CH CH CH CH d) OH OH 13....
HO CH сн. CH2 нс HC CH3 HAC-HC CH CH CH CH d) OH OH 13. The labels have fallen off three bottles. Bottle A contains a gas, bottle B contains a liquid, and bottle C contains a solid. The labels indicate that the compounds have the same number of carbon atoms, one being an alkane, one an alcohol, and the other a carboxylic acid. Suggest the identity of the contents of each bottle, and give reasons for your explanation...
Answer the following questions with only one answer a. Carboxylic acid derivatives cannot be hydrolyzed to...
Answer the following questions with only one answer a. Carboxylic acid derivatives cannot be hydrolyzed to produce carboxylic acids b. Lithium aluminum (tri-butoxy)hydride will convert acid chlorides to ketones c. Amides have more resonance stability than esters d. Nitriles are less basic than primary amines e. Grignard reagents contain polar covalent carbon-magnesium bonds f. Anhydrides are more reactive than esters in nucleophilic acyl substitution reactions g. Acid chlorides undergo nucleophilic acyl substitution reactions h. Nitriles have an sp hybridized Nitrogen...
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...
please answer b *PLEASE DO NOT FORGET THE EXPLANATION* b. Circle the most likely structure that...
please answer b
*PLEASE DO NOT FORGET THE EXPLANATION*
b. Circle the most likely structure that corresponds to the IR spectrum: Spectrum: Explanation (be specific): Infrared Absorption Bands Frequency (cm ) Type of Vibration Intensity C-H Alkanes -CH -CH2- Alkenes (stretch) (bend) (bend) (stretch) (out-of-plane bend) (stretch) (out-of-plane bend) (stretch) Aromatics 3000-2850 1450 and 1375 1465 3100-3000 1000-650 3150-3050 900-690 ca. 3300 2900-2800 2800-2700 Alkyne Aldehyde O-H Alcohol, phenols Free H-bonded Carboxylic acids Primary and secondary amines and amides (stretch)...
____ 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...
INFRARED SPECTROSCOPY 1. Circle AND label the functional groups in each molecule. Then predict the signal(s)...
INFRARED SPECTROSCOPY
1. Circle AND label the functional groups in
each molecule. Then predict the signal(s) that
would result from each functional group in the IR.
PLEASE ANSWER (C) and (D please follow the directions
and write neatly
Но, ес -CEC-H Infrared Absorption Bands Type of Vibration Frequency (cm21) Intensity C-H Alkanes CH CH- Alkenes (stretch) (bend) (bend) (stretch) (out-of-plane bend) (stretch) (out-of-plane bend) (stretch) Aromatics 3000-2850 1450 and 1375 1465 3100-3000 1000-650 3150-3050 900-690 ca. 3300 2900-2800 2800-2700 Alkyne...
What kinds of interactions are NOT part of tertiary protein structure? 3 . A) salt bridges...
What kinds of interactions are NOT part of tertiary protein structure? 3 . A) salt bridges In a hydrolysis reaction, B) hydrophilic interactions A. an acid reacts with an alcohol. C) disulfide bonds E. an este reacts with NaOH. C. anester reacts with H.O. D) peptide bonds D. an acid neutralizes a base. E) hydrophobic interactions E. water is added to markene. . All amino acids have chiral Carbon atoms except a. Val 6. Lys C. ASP d. Ala e....
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...
Questions and Problems 553 ation for the reaction that would produse cach of the following amines...
Questions and Problems 553 ation for the reaction that would produse cach of the following amines b. N.Methylpropanamine c. N.N-Diethylpentanamine 15.37 Briefly explain why the lower molar massamines (lewer than five carbons) exhibit appreciable solubility in water 15.38 Why is the salt of an amine appreciably more soluble in water than the mine from which it was formed 15.39 Most drugs containing amine groups are not administered as the mine but rather the amount you suggeste son why? 15.40 Why...
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...
HO CH сн. CH2 нс HC CH3 HAC-HC CH CH CH CH d) OH OH 13. The labels have fallen off three bottles. Bottle A contains a gas, bottle B contains a liquid, and bottle C contains a solid. The labels indicate that the compounds have the same number of carbon atoms, one being an alkane, one an alcohol, and the other a carboxylic acid. Suggest the identity of the contents of each bottle, and give reasons for your explanation...
Answer the following questions with only one answer a. Carboxylic acid derivatives cannot be hydrolyzed to produce carboxylic acids b. Lithium aluminum (tri-butoxy)hydride will convert acid chlorides to ketones c. Amides have more resonance stability than esters d. Nitriles are less basic than primary amines e. Grignard reagents contain polar covalent carbon-magnesium bonds f. Anhydrides are more reactive than esters in nucleophilic acyl substitution reactions g. Acid chlorides undergo nucleophilic acyl substitution reactions h. Nitriles have an sp hybridized Nitrogen...
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...
please answer b
*PLEASE DO NOT FORGET THE EXPLANATION*
b. Circle the most likely structure that corresponds to the IR spectrum: Spectrum: Explanation (be specific): Infrared Absorption Bands Frequency (cm ) Type of Vibration Intensity C-H Alkanes -CH -CH2- Alkenes (stretch) (bend) (bend) (stretch) (out-of-plane bend) (stretch) (out-of-plane bend) (stretch) Aromatics 3000-2850 1450 and 1375 1465 3100-3000 1000-650 3150-3050 900-690 ca. 3300 2900-2800 2800-2700 Alkyne Aldehyde O-H Alcohol, phenols Free H-bonded Carboxylic acids Primary and secondary amines and amides (stretch)...
____ 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...
INFRARED SPECTROSCOPY
1. Circle AND label the functional groups in
each molecule. Then predict the signal(s) that
would result from each functional group in the IR.
PLEASE ANSWER (C) and (D please follow the directions
and write neatly
Но, ес -CEC-H Infrared Absorption Bands Type of Vibration Frequency (cm21) Intensity C-H Alkanes CH CH- Alkenes (stretch) (bend) (bend) (stretch) (out-of-plane bend) (stretch) (out-of-plane bend) (stretch) Aromatics 3000-2850 1450 and 1375 1465 3100-3000 1000-650 3150-3050 900-690 ca. 3300 2900-2800 2800-2700 Alkyne...
What kinds of interactions are NOT part of tertiary protein structure? 3 . A) salt bridges In a hydrolysis reaction, B) hydrophilic interactions A. an acid reacts with an alcohol. C) disulfide bonds E. an este reacts with NaOH. C. anester reacts with H.O. D) peptide bonds D. an acid neutralizes a base. E) hydrophobic interactions E. water is added to markene. . All amino acids have chiral Carbon atoms except a. Val 6. Lys C. ASP d. Ala e....
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...
Questions and Problems 553 ation for the reaction that would produse cach of the following amines b. N.Methylpropanamine c. N.N-Diethylpentanamine 15.37 Briefly explain why the lower molar massamines (lewer than five carbons) exhibit appreciable solubility in water 15.38 Why is the salt of an amine appreciably more soluble in water than the mine from which it was formed 15.39 Most drugs containing amine groups are not administered as the mine but rather the amount you suggeste son why? 15.40 Why...
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...
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