
Biochemistry
9th Edition
ISBN: 9781319114671
Author: Lubert Stryer, Jeremy M. Berg, John L. Tymoczko, Gregory J. Gatto Jr.
Publisher: W. H. Freeman
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![46
2 H
G
CI
8 Is M (n G e
M In
In
VI
LE
Q S
M In b M X
+
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A canvas.northseattle.edu/courses/2086259/quizzes/5876542/take
H
H
N-C-C
H
он
CH
CH,
CH,
Account
H,C
Dashboard
Courses
The monomer above is a(n) [Select]
The changeable side group
Groups
in this example is [ Select ]
Calendar
In order to form a polymer from many of these monomers,
[ Select ]
would need to occur.
Inbox
The polymer that is formed by joining these monomers together is called a
[ Select ]
. whereas the functional molecule made of this
History
monomer is called a [Select]
Help
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Transcribed Image Text:46
2 H
G
CI
8 Is M (n G e
M In
In
VI
LE
Q S
M In b M X
+
uv
A canvas.northseattle.edu/courses/2086259/quizzes/5876542/take
H
H
N-C-C
H
он
CH
CH,
CH,
Account
H,C
Dashboard
Courses
The monomer above is a(n) [Select]
The changeable side group
Groups
in this example is [ Select ]
Calendar
In order to form a polymer from many of these monomers,
[ Select ]
would need to occur.
Inbox
The polymer that is formed by joining these monomers together is called a
[ Select ]
. whereas the functional molecule made of this
History
monomer is called a [Select]
Help
3 •1 8:17
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- Rotation about the peptide bond in glycylalanine is hindered. Draw the resonance forms of the peptide bond and explain why.arrow_forwardThis macromolecule is readily available and used extensively.The molecule below is a H H HHH C-H H-C-o HHHH HHHH HHHH H H C-C -C-C H-C-o HHHH H H H H HHH H. H H o-0-H a saturated fatty acid amino acid monounsaturated fatty acid O triglyceride O polyunsaturated fatty acid I-o-z I-O-I I-O-I I-0-I I-O-I I-0-Iarrow_forwardConsider this structure. CH₂OH HO Part 1 of 3 NH Identify the monosaccharide. Select the single best answer. D-2-deoxyribose D-ribose Part 2 of 3 Identify the base. Select the single best answer. thymine guanine cytosine adenine Ouracil Part: 2/3 Part 3 of 3 Name the structure. х NH₂arrow_forward
- The monosaccharide shown below is the CH₂OH OH OH beta- L- D- alpha- Он OH anomer.arrow_forwardIdentify the primary structure of a hexapeptide containing five different amino acids if the following smaller peptides are among the partial hydrolysis products: Gly-Cys, Ala-Ser, Ala-Gly, and Cys-Val-Alaarrow_forwardHighlight all polar bonds. If applicable, be sure to highlight all bonds in a double or triple bond. If there are no polar bonds, please check the box below. Harrow_forward
- a. what general category would you place this molecule in of the four categories of biomolecules? b. List 5 functional groups you see in this molecule?arrow_forwardCH;OH НО OH What is the name of this structure? OH OH alpha-D-gulopryranose O beta-L-gulofuransone O alpha-L-gulofuranose beta-D- gulopyranosearrow_forwardThreonine has two chiral centers. Draw L-threonine and indicate which carbon atoms are chiral. Which carbon atom is responsible for d and L configuration?arrow_forward
- In the peptide shown below, a covalent bond that could rotate to form secondary structure is correctly identified / labeled by letter: A B OH still fot D OB OC O O O B D F C OA HN E NH OH "NH₂ - Farrow_forwardIndicate next to each letter the name of the monomers shown below and write the name of the polymer that is produced from the monomer. H-C-OH HỌ-C-H H-C-OH H-C-OH о- 6 CH₂OH 0=P-O О CH₂ Phosphate H group А: Name of polymer: H- Н Н OH H Sugar Н Н. H Nitrogenous base (adenine) C: 0 НО Name of polymer: H C-C-N CH2 SH Н НИ Н III H-N-С-С-0 +111 НКН н B: Name of polymer: Н 0 0-C-H o Н-С-0² H-C-O H S ННННННННННН Н Н Н LI -CH Н ННННННННННН Н Н Н ITIILE I C-C H ...... С-с-с-с-с-с-с III E .. ННННННННННН Н Н С-С-f 111 1 FE D: I НННННННННННННН No polymer!arrow_forwardConsider this structure. NH₂ N N O P O N N Part 1 of 3 HO Identify the monosaccharide. Select the single best answer. D-ribose D-2-deoxyribose Part: 1/3 Part 2 of 3 Identify the base. Select the single best answer. Othymine O guanine ○ cytosine adenine uracilarrow_forward
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