Chemistry
Chemistry
10th Edition
ISBN: 9781305957404
Author: Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher: Cengage Learning
Bartleby Related Questions Icon

Related questions

Question
9. For the DNA segment with nucleotide sequence 5' TATCGC 3’, how many hydrogen
bonds in total hold the base pairs between this segment and its complementary strand?
А. 5
В.
6
С. 15
D. 18
E. Cannot be determined
10. What is the relation between the Fischer projection of two molecules below?
H
H-
-OH
Но-
но-
H-
Но
H-
H-
-OH-
Но-
CH2OH
CH2OH
A. C2 epimers
В. СЗ ерimers
C. Enantiomers
D. Anomers
E. Superimposable molecules
Section B: True / False (10 marks)
A group is deprotonated when its pKa value is lower than the pH of
the solution.
1.
T or F
2.
a and B configurations are used to describe enantiomers.
T or F
3.
Hydrogen bond can be formed between two peptide bonds.
T or F
4.
A single strand of RNA has 20% U so it also has 20% A.
T or F
5.
Arginine's pI lies between 2.34 and 9.6.
T or F
6.
O-6 fatty acids have fewer double bonds than @-9 fatty acids have.
T or F
7.
The net charge of glycine changes at different pH.
T or F
8.
The hydroxyl group in threonine is deprotonated at high pH.
T or F
9.
Deoxyguanosine contains a monophosphate.
T or F
10. Ketohexose gives positive result in Benedict's test.
T or F
3
expand button
Transcribed Image Text:9. For the DNA segment with nucleotide sequence 5' TATCGC 3’, how many hydrogen bonds in total hold the base pairs between this segment and its complementary strand? А. 5 В. 6 С. 15 D. 18 E. Cannot be determined 10. What is the relation between the Fischer projection of two molecules below? H H- -OH Но- но- H- Но H- H- -OH- Но- CH2OH CH2OH A. C2 epimers В. СЗ ерimers C. Enantiomers D. Anomers E. Superimposable molecules Section B: True / False (10 marks) A group is deprotonated when its pKa value is lower than the pH of the solution. 1. T or F 2. a and B configurations are used to describe enantiomers. T or F 3. Hydrogen bond can be formed between two peptide bonds. T or F 4. A single strand of RNA has 20% U so it also has 20% A. T or F 5. Arginine's pI lies between 2.34 and 9.6. T or F 6. O-6 fatty acids have fewer double bonds than @-9 fatty acids have. T or F 7. The net charge of glycine changes at different pH. T or F 8. The hydroxyl group in threonine is deprotonated at high pH. T or F 9. Deoxyguanosine contains a monophosphate. T or F 10. Ketohexose gives positive result in Benedict's test. T or F 3
Section C: Short Questions
1. Consider the peptide with amino acid sequence NICE.
а.
Write the full name and the three-letter abbreviations of the amino acids in the
(8 marks)
Calculate the net charge of the peptide at pH 7.0. Show you work in a table. Step
(3 marks)
Calculate the pI of the peptide. Show you work in a table. Step marks are counted.
(6 marks)
peptide.
b.
marks are counted.
с.
2. Write the full name of amino acids, from N-terminus to C-terminus, after hydrolysis of
the following polypeptide. How many peptide bonds are present?
(5 marks)
H,N-CH-C-
CH-
CH-C
N-CH-C-0-
H,C-CH
H CH,
CH2
H ČH,-C-NH,
ČH
H
3. Complete the following table. (9 marks; 0.5 mark @ for a-d, 1 mark @ for e)
а.
СНО
b.
CH,OH
СНО
с.
HO-H
HO
-H-
C=0
H-
-OH
H-
-O-
H
-O-
HO-H
HO-*H
Нон
CH,OH
HO-H
HO-*H
CH,OH
CH-OH
a. Number of
chiral carbon
b. D or L
configuration
c. Aldose or
ketose?
d. If the -OH of
carbon with *
forms a bond
with the carbon
of the carbonyl
group, the cyclic
form will be a
furanose or
pyranose?
4
expand button
Transcribed Image Text:Section C: Short Questions 1. Consider the peptide with amino acid sequence NICE. а. Write the full name and the three-letter abbreviations of the amino acids in the (8 marks) Calculate the net charge of the peptide at pH 7.0. Show you work in a table. Step (3 marks) Calculate the pI of the peptide. Show you work in a table. Step marks are counted. (6 marks) peptide. b. marks are counted. с. 2. Write the full name of amino acids, from N-terminus to C-terminus, after hydrolysis of the following polypeptide. How many peptide bonds are present? (5 marks) H,N-CH-C- CH- CH-C N-CH-C-0- H,C-CH H CH, CH2 H ČH,-C-NH, ČH H 3. Complete the following table. (9 marks; 0.5 mark @ for a-d, 1 mark @ for e) а. СНО b. CH,OH СНО с. HO-H HO -H- C=0 H- -OH H- -O- H -O- HO-H HO-*H Нон CH,OH HO-H HO-*H CH,OH CH-OH a. Number of chiral carbon b. D or L configuration c. Aldose or ketose? d. If the -OH of carbon with * forms a bond with the carbon of the carbonyl group, the cyclic form will be a furanose or pyranose? 4
Expert Solution
Check Mark
Knowledge Booster
Background pattern image
Chemistry
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.
Similar questions
SEE MORE QUESTIONS
Recommended textbooks for you
Text book image
Chemistry
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning
Text book image
Chemistry
Chemistry
ISBN:9781259911156
Author:Raymond Chang Dr., Jason Overby Professor
Publisher:McGraw-Hill Education
Text book image
Principles of Instrumental Analysis
Chemistry
ISBN:9781305577213
Author:Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:Cengage Learning
Text book image
Organic Chemistry
Chemistry
ISBN:9780078021558
Author:Janice Gorzynski Smith Dr.
Publisher:McGraw-Hill Education
Text book image
Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
Publisher:Cengage Learning
Text book image
Elementary Principles of Chemical Processes, Bind...
Chemistry
ISBN:9781118431221
Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:WILEY