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Refer to image below: How many peptide bonds are there? Refer to image below: Locate the chiral carbon. (Carbons are labelled in capital letters) Choose Choose NH A Alkyl B. Sulfide c. Guanidine A Leucine B Methionine C. Arginine HN HO. A. Alkyl B. Thiol C. Amino A. Isoleucine B. Cysteine C. Lysine NH, A Ethylene . Thiol C. Amino A. Pseudo Amino Acid B. Cysteine c. Lysine A Alkyl B. Sulfide C. Amino A. Leucine B. Cysteine C. Lysine Choose Refer to image below: What type of peptide is it? Refer to image below: Which group becomes acidic when ethanoic acid is added in the system? Refer to image below: Which requires more base to transform to its zwitterion form? * Refer to image below: Which group is acidic? Choose Choose Фреptide hich requires more witterion form? tripeptide Choose polypeptide

Refer to image below: How many peptide bonds are there? Refer to image below: Locate the chiral carbon. (Carbons are labelled in capital letters) Choose Choose NH A Alkyl B. Sulfide c. Guanidine A Leucine B Methionine C. Arginine HN HO. A. Alkyl B. Thiol C. Amino A. Isoleucine B. Cysteine C. Lysine NH, A Ethylene . Thiol C. Amino A. Pseudo Amino Acid B. Cysteine c. Lysine A Alkyl B. Sulfide C. Amino A. Leucine B. Cysteine C. Lysine Choose Refer to image below: What type of peptide is it? Refer to image below: Which group becomes acidic when ethanoic acid is added in the system? Refer to image below: Which requires more base to transform to its zwitterion form? * Refer to image below: Which group is acidic? Choose Choose Фреptide hich requires more witterion form? tripeptide Choose polypeptide

Chemistry
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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RECOVERED UNSAVED FILE This is a recovered file that is temporarily stored on your computer. Save Refer to image below: How many peptide bonds are there? * Refer to image below: Locate the chiral carbon. (Carbons are labelled in capital letters) Choose Choose NH A. Alkyl B. Sulfide C. Guanidino A. Leucine B. Methionine C. Arginine HN HO A. Alkyl B. Thiol C. Amino A. Isoleucine B. Cysteine C. Lysine NH2 nino A. Ethylene B. Thiol C. Amino A. Pseudo Amino Acid B. Cysteine C. Lysine A. Alkyl B. Sulfide C. Amino A. Leucine B. Cysteine C. Lysine Choose Refer to image below: What type of peptide is it? to image below: Which group becomes acidic when ethanoic acid is added in the system? Refer to image below: Which requires more base to transform to its zwitterion form? * Refer to image below: Which group is Choose acidic? Choose HC. dipeptide hich requires more witterion form? 0-H tripeptide Choose polypeptide 10:14 am P Type here to search A O A 4) ENG 25/09/2021
Transcribed Image Text:RECOVERED UNSAVED FILE This is a recovered file that is temporarily stored on your computer. Save Refer to image below: How many peptide bonds are there? * Refer to image below: Locate the chiral carbon. (Carbons are labelled in capital letters) Choose Choose NH A. Alkyl B. Sulfide C. Guanidino A. Leucine B. Methionine C. Arginine HN HO A. Alkyl B. Thiol C. Amino A. Isoleucine B. Cysteine C. Lysine NH2 nino A. Ethylene B. Thiol C. Amino A. Pseudo Amino Acid B. Cysteine C. Lysine A. Alkyl B. Sulfide C. Amino A. Leucine B. Cysteine C. Lysine Choose Refer to image below: What type of peptide is it? to image below: Which group becomes acidic when ethanoic acid is added in the system? Refer to image below: Which requires more base to transform to its zwitterion form? * Refer to image below: Which group is Choose acidic? Choose HC. dipeptide hich requires more witterion form? 0-H tripeptide Choose polypeptide 10:14 am P Type here to search A O A 4) ENG 25/09/2021
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