The structural formula tur alutamic acid is -CH-CH-CH- C HO NH. 23. The systanic name for glutamic acid is A) 4 - amino pentanedioic acid B) 2- aminopenta -1, 5- dioic acid C) 2 - amino propan - 1, 3- dioic acid D) 4 - amino pentan -1, 5 - dioic acid D4. In what major class of organic compounds does glutamic acid belong? A) amino acids. B) dicarboxylic acids C) proteins D) dipetide 25. What is the structure of the more common form of this compound in aqueous solution C-CH,-CH-CH- A) o NH, B) C-CH,-CH-CH-C
The structural formula tur alutamic acid is -CH-CH-CH- C HO NH. 23. The systanic name for glutamic acid is A) 4 - amino pentanedioic acid B) 2- aminopenta -1, 5- dioic acid C) 2 - amino propan - 1, 3- dioic acid D) 4 - amino pentan -1, 5 - dioic acid D4. In what major class of organic compounds does glutamic acid belong? A) amino acids. B) dicarboxylic acids C) proteins D) dipetide 25. What is the structure of the more common form of this compound in aqueous solution C-CH,-CH-CH- A) o NH, B) C-CH,-CH-CH-C
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Answer Q23, 24 25
![Questions 28-30
The structural formula tur alutamic acid is
29. When CH CN is refluxed with aqueous KOFH
the prinicipa organic product is
A) CH OH
C) CH CONH, Dy CH CH OH
30. Which one of the following substances
shows amphoteric character most
prominently?
A) CH COONH, B) C,H,NH,
C) CH CONH D) H.NCH COOH
C-CH CH-CH1-
HO
B) CH COO
NH.
23. The systamic name for glutamic acid is
A) 4 - amino pentanedioic acid
B) 2- aminopenta -1, 5- dioic acid
C) 2 - amino propan - 1, 3 - dioic acid
D) 4 - amino pentan -1,5 - dioic acid
HO
24.
In what major class of organic compounds
D) dipetide
25. What is the structure of the more common
form of this compound in aqueous solution
does glutamic acid belong?
A) amino acids. B) dicarboxylic acids
C) proteins
31. Which of the following is, the main organic
product when ammonium propanoate is
heated with P O, ?
A) ethanenitrile B) propanamide
C) propanenitrile D) propanoic acid
-CH-CH-GİI-C
32. Which of the following terms best describes
nylon?
A) natural fibre
A)
NH,
B) synthetic protein
C) condensation polymer
D) natural polyamide
B)
CH-CH- CH-
NH,
HO
33. Aminoethanoic acid, H,NCH COOH,
(Mr=75) melts at 234°C, whereas propanoic
acid CH,CH COOH, (Mr = 74) melts at -
21 C. Which of the following statements
helps to explain this difference?
Amino ethanoic acid molecules are;
A) hydrogen bonded
B) dimarized
C) having dipole-dipole intereaction
D) having a dipolar ion struclure.
C-CH-CH-
HO
NH,
CH-CH
+2H
NH,
Questions 26 and 27
Consider the reaction
NaNO, (ag).H
CH CH,CONH,
R
34. What is the IUPAC namefor the compound
with structure
26. Give the reagents for step "a"
A) Br/OH(aq)
C) NaOH
27. The structural formula of R and S are
repectively
A) CH,CH CH NH, and CH,CH,CH,N,
B) CH CH NH, and CH,CH
C) CH CH NH, and CH CH.OH
D) CH,CH CH NH, and CH,CH.CH,OH
B) HNO,
D) HCI(aq)
CH,CHCH,?
CN
A) 2-propanenitrile
B) propane - 2- nitrile
C) 2 - butanenitrile
C) 2- methylpropanenitrile
35. Which one of the following reagents would
be the most suitable for carrving out the
conversion below
28. The order of increasing strength as bases
for aimethylamine, methylamine and
phenylamine is
A) dimethylamine, methylamine and
phenylamine
B) methylamine, dimethylamine and
phenylamine
C) phenylamine, dimethylamine and
methylamine
D) pheylamine, methylamine and
dimethylamine
H,C-(O N C
A) chlorine gas in sunlight
B) chlorine gas and a halogen carrier
C) copper!l) chloride and hydrochloric acid
D) phosphorus pentachloride.
HC-O CI
363](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F5a6d9c67-6f13-49d2-ac4d-2d996f90a88b%2Feebcd628-d364-4ce6-a81b-2b9591ed5339%2Fqdxp40g_processed.jpeg&w=3840&q=75)
Transcribed Image Text:Questions 28-30
The structural formula tur alutamic acid is
29. When CH CN is refluxed with aqueous KOFH
the prinicipa organic product is
A) CH OH
C) CH CONH, Dy CH CH OH
30. Which one of the following substances
shows amphoteric character most
prominently?
A) CH COONH, B) C,H,NH,
C) CH CONH D) H.NCH COOH
C-CH CH-CH1-
HO
B) CH COO
NH.
23. The systamic name for glutamic acid is
A) 4 - amino pentanedioic acid
B) 2- aminopenta -1, 5- dioic acid
C) 2 - amino propan - 1, 3 - dioic acid
D) 4 - amino pentan -1,5 - dioic acid
HO
24.
In what major class of organic compounds
D) dipetide
25. What is the structure of the more common
form of this compound in aqueous solution
does glutamic acid belong?
A) amino acids. B) dicarboxylic acids
C) proteins
31. Which of the following is, the main organic
product when ammonium propanoate is
heated with P O, ?
A) ethanenitrile B) propanamide
C) propanenitrile D) propanoic acid
-CH-CH-GİI-C
32. Which of the following terms best describes
nylon?
A) natural fibre
A)
NH,
B) synthetic protein
C) condensation polymer
D) natural polyamide
B)
CH-CH- CH-
NH,
HO
33. Aminoethanoic acid, H,NCH COOH,
(Mr=75) melts at 234°C, whereas propanoic
acid CH,CH COOH, (Mr = 74) melts at -
21 C. Which of the following statements
helps to explain this difference?
Amino ethanoic acid molecules are;
A) hydrogen bonded
B) dimarized
C) having dipole-dipole intereaction
D) having a dipolar ion struclure.
C-CH-CH-
HO
NH,
CH-CH
+2H
NH,
Questions 26 and 27
Consider the reaction
NaNO, (ag).H
CH CH,CONH,
R
34. What is the IUPAC namefor the compound
with structure
26. Give the reagents for step "a"
A) Br/OH(aq)
C) NaOH
27. The structural formula of R and S are
repectively
A) CH,CH CH NH, and CH,CH,CH,N,
B) CH CH NH, and CH,CH
C) CH CH NH, and CH CH.OH
D) CH,CH CH NH, and CH,CH.CH,OH
B) HNO,
D) HCI(aq)
CH,CHCH,?
CN
A) 2-propanenitrile
B) propane - 2- nitrile
C) 2 - butanenitrile
C) 2- methylpropanenitrile
35. Which one of the following reagents would
be the most suitable for carrving out the
conversion below
28. The order of increasing strength as bases
for aimethylamine, methylamine and
phenylamine is
A) dimethylamine, methylamine and
phenylamine
B) methylamine, dimethylamine and
phenylamine
C) phenylamine, dimethylamine and
methylamine
D) pheylamine, methylamine and
dimethylamine
H,C-(O N C
A) chlorine gas in sunlight
B) chlorine gas and a halogen carrier
C) copper!l) chloride and hydrochloric acid
D) phosphorus pentachloride.
HC-O CI
363
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