Organic And Biological Chemistry
7th Edition
ISBN: 9781305081079
Author: STOKER, H. Stephen (howard Stephen)
Publisher: Cengage Learning,
expand_more
expand_more
format_list_bulleted
Concept explainers
Question
Chapter 15.8, Problem 4QQ
Interpretation Introduction
Interpretation: To identify a nonmetabolic function for hydrogen sulfide.
Concept introduction: Cysteine is a nonessential amino acid and has a sulfur atom in its side chain. The structure of cysteine is:
In degradation of the sulfur-containing amino acid cysteine, the sulfur is released in the form of hydrogen sulfide. The degradation process of cysteine is as follows:
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
Which of the following hormones increases blood glucose levels?
a. glucagon and epinephrine
b. insulin and epinephrine
c. insulin and glucagon
d. more than one correct response
e. no correct response
HO,
N'
Steric effect
A) Present
B) Absent
22. According to the lock-and-key theory of enzyme behavior, which of the following can be thought of as the key?
a. enzyme
b. substrate
с. ароenzyme
d. coenzyme
e. no correct response
Chapter 15 Solutions
Organic And Biological Chemistry
Ch. 15.1 - Which of the following statements about dietary...Ch. 15.1 - Dietary protein materials as they leave the...Ch. 15.1 - Prob. 3QQCh. 15.1 - Which of the following is not a proteolytic...Ch. 15.2 - The dominant use for the amino acids of the amino...Ch. 15.2 - The most abundant amino acid in the amino acid...Ch. 15.2 - Prob. 3QQCh. 15.3 - The reactants in a transamination reaction are a....Ch. 15.3 - Prob. 2QQCh. 15.3 - Prob. 3QQ
Ch. 15.3 - Prob. 4QQCh. 15.3 - Prob. 5QQCh. 15.3 - Prob. 6QQCh. 15.4 - Prob. 1QQCh. 15.4 - Prob. 2QQCh. 15.4 - Prob. 3QQCh. 15.4 - Prob. 4QQCh. 15.4 - Prob. 5QQCh. 15.4 - In the urea cycle, the urea-producing step...Ch. 15.5 - Which of the following statements concerning the...Ch. 15.5 - Prob. 2QQCh. 15.5 - Which of the following statements concerning the...Ch. 15.5 - Prob. 4QQCh. 15.6 - Prob. 1QQCh. 15.6 - Prob. 2QQCh. 15.6 - Prob. 3QQCh. 15.7 - Prob. 1QQCh. 15.7 - Prob. 2QQCh. 15.7 - In the degradation of heme, which of the following...Ch. 15.7 - In the degradation of heme, the iron atom present...Ch. 15.8 - In degradation of the sulfur-containing amino acid...Ch. 15.8 - Prob. 2QQCh. 15.8 - Prob. 3QQCh. 15.8 - Prob. 4QQCh. 15.9 - Prob. 1QQCh. 15.9 - Prob. 2QQCh. 15.9 - Prob. 3QQCh. 15.10 - Transamination reactions require the cofactor PLP...Ch. 15.10 - Prob. 2QQCh. 15.10 - Prob. 3QQCh. 15 - Prob. 15.1EPCh. 15 - Indicate whether each of the following aspects of...Ch. 15 - Prob. 15.3EPCh. 15 - Prob. 15.4EPCh. 15 - Prob. 15.5EPCh. 15 - Prob. 15.6EPCh. 15 - Prob. 15.7EPCh. 15 - Prob. 15.8EPCh. 15 - Prob. 15.9EPCh. 15 - Prob. 15.10EPCh. 15 - Prob. 15.11EPCh. 15 - Prob. 15.12EPCh. 15 - Prob. 15.13EPCh. 15 - Indicate whether each of the following statements...Ch. 15 - Prob. 15.15EPCh. 15 - Prob. 15.16EPCh. 15 - Prob. 15.17EPCh. 15 - What are the four major uses for amino acids...Ch. 15 - With the help of Table 26-1, classify each of the...Ch. 15 - Prob. 15.20EPCh. 15 - Prob. 15.21EPCh. 15 - Prob. 15.22EPCh. 15 - Prob. 15.23EPCh. 15 - Prob. 15.24EPCh. 15 - Prob. 15.25EPCh. 15 - Prob. 15.26EPCh. 15 - Prob. 15.27EPCh. 15 - Prob. 15.28EPCh. 15 - Prob. 15.29EPCh. 15 - Prob. 15.30EPCh. 15 - Prob. 15.31EPCh. 15 - Prob. 15.32EPCh. 15 - Prob. 15.33EPCh. 15 - Prob. 15.34EPCh. 15 - Prob. 15.35EPCh. 15 - Prob. 15.36EPCh. 15 - Prob. 15.37EPCh. 15 - Prob. 15.38EPCh. 15 - Prob. 15.39EPCh. 15 - Prob. 15.40EPCh. 15 - Prob. 15.41EPCh. 15 - Prob. 15.42EPCh. 15 - Draw the structure of the -keto acid produced from...Ch. 15 - Draw the structure of the -keto acid produced from...Ch. 15 - Prob. 15.45EPCh. 15 - Prob. 15.46EPCh. 15 - Prob. 15.47EPCh. 15 - Prob. 15.48EPCh. 15 - Prob. 15.49EPCh. 15 - Prob. 15.50EPCh. 15 - Prob. 15.51EPCh. 15 - Prob. 15.52EPCh. 15 - Prob. 15.53EPCh. 15 - Prob. 15.54EPCh. 15 - What is a carbamoyl group?Ch. 15 - Prob. 15.56EPCh. 15 - Prob. 15.57EPCh. 15 - Prob. 15.58EPCh. 15 - Prob. 15.59EPCh. 15 - Prob. 15.60EPCh. 15 - Prob. 15.61EPCh. 15 - Prob. 15.62EPCh. 15 - Prob. 15.63EPCh. 15 - Prob. 15.64EPCh. 15 - Prob. 15.65EPCh. 15 - Prob. 15.66EPCh. 15 - Prob. 15.67EPCh. 15 - Prob. 15.68EPCh. 15 - Prob. 15.69EPCh. 15 - Prob. 15.70EPCh. 15 - Prob. 15.71EPCh. 15 - Prob. 15.72EPCh. 15 - Prob. 15.73EPCh. 15 - Prob. 15.74EPCh. 15 - Prob. 15.75EPCh. 15 - Prob. 15.76EPCh. 15 - Prob. 15.77EPCh. 15 - Prob. 15.78EPCh. 15 - Prob. 15.79EPCh. 15 - Prob. 15.80EPCh. 15 - Prob. 15.81EPCh. 15 - Prob. 15.82EPCh. 15 - Prob. 15.83EPCh. 15 - Prob. 15.84EPCh. 15 - Prob. 15.85EPCh. 15 - Prob. 15.86EPCh. 15 - Prob. 15.87EPCh. 15 - What is the starting material for the biosynthesis...Ch. 15 - Prob. 15.89EPCh. 15 - Prob. 15.90EPCh. 15 - Prob. 15.91EPCh. 15 - Prob. 15.92EPCh. 15 - Prob. 15.93EPCh. 15 - What are the structural differences between...Ch. 15 - Prob. 15.95EPCh. 15 - Prob. 15.96EPCh. 15 - Which bile pigment is responsible for the yellow...Ch. 15 - Prob. 15.98EPCh. 15 - Prob. 15.99EPCh. 15 - Prob. 15.100EPCh. 15 - Prob. 15.101EPCh. 15 - Prob. 15.102EPCh. 15 - Prob. 15.103EPCh. 15 - Prob. 15.104EPCh. 15 - Prob. 15.105EPCh. 15 - Indicate whether each of the following statements...Ch. 15 - Prob. 15.107EPCh. 15 - Prob. 15.108EPCh. 15 - Prob. 15.109EPCh. 15 - Prob. 15.110EPCh. 15 - Prob. 15.111EPCh. 15 - Prob. 15.112EPCh. 15 - Prob. 15.113EPCh. 15 - Prob. 15.114EPCh. 15 - Prob. 15.115EPCh. 15 - Prob. 15.116EP
Knowledge Booster
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
- 24. CH3-NH-CH3 The compound above would be classified as a O primary Osecondary O tertiary O quaternary 25. NH₂ I A correct IUPAC name for CH₂-CH₂-C-CH3 O 3-methyl-3-hexanamine 2-propyl-2-butanamine 2-ethyl-2-pentanamine O no correct response CH₂-CH₂-CH3 is aminearrow_forward22. The complete hydrolysis of a protein yields what as products? a. amino acids b. dipeptides C. monosaccharides d. glucose molecules e. no correct responsearrow_forwardWhat are the functional groups for the Qualitative Tests for carbonyls and Unknown Carbonyl.arrow_forward
- What is the [A2-] (in mol L-1) of a solution containing 1.448 mol L-1 of a diprotic acid with pKA1 = 3 and PKA2 = 9.92 ? H₂A + H₂O H3O+ + HA PKA1 HA + H₂O = H3O+ + A²- pkA2 Answer:arrow_forward9. Which of the following amines is paired with an incorrect IUPAC name? a CH3-CH-NH21-methylethanamine CH3 b. CH3-CH2-NH-CH,; N-methylethan amine C. CH3-CH2-CH-CH3; 2-butanamine NH2 d. more than one correct response e. no correct responsearrow_forwardStudy guide 29 Option A.)[Option 1] “Shift A” Option B.) [Option 2] “Shift B”arrow_forward
- amHUniuml Cation. What products are formed when each of the following amines is treated with HCI: (a) CH,CH¸NH,; (b) (CH,CH,),NH; (c) (CH,CH,),N? Practice Problem 18.4 More Practice: Try Problems 18.51, 18.53, 18.54, 18.73g, 18.74f.arrow_forward24. In the following diagram, the rate of an enzyme-catalyzed reaction is graphed on the y (or vertical) axis versus another quantity on the x axis. What quantity is graphed on the x axis? a. substrate concentration Ob. reaction pH Oc. reaction temperature Od. more than one response is correct e. no correct responsearrow_forward> ▼ Part A Identify the compound that is in nail polish remover. O butanone Obutanal O benzaldehyde O acetone Ovanillin Submit Provide Feedback Request Answerarrow_forward
- What two chemicals can be reacted together to fom an ester? A- An alcohol and a carboxylic acid B- A carboxylic acid and an alkali C- Two carboxylic acids D-Non of these Answer A Answer B Answer C Answer Darrow_forwardPart A High blood levels of LDL-cholesterol increase the risk of cardiovascular disease. O True O False Submit Request Answer vide Feedbackarrow_forwardWhich of the following is NOT a use of aromatic hydrocarbons? a. solvents b. found in vitamins c. found in amino acids d. no correct responsearrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
General, Organic, and Biological ChemistryChemistryISBN:9781285853918Author:H. Stephen StokerPublisher:Cengage Learning
Organic And Biological ChemistryChemistryISBN:9781305081079Author:STOKER, H. Stephen (howard Stephen)Publisher:Cengage Learning,
General, Organic, and Biological Chemistry
Chemistry
ISBN:9781285853918
Author:H. Stephen Stoker
Publisher:Cengage Learning
Organic And Biological Chemistry
Chemistry
ISBN:9781305081079
Author:STOKER, H. Stephen (howard Stephen)
Publisher:Cengage Learning,