Concept explainers
(a)
Interpretation:
In the
Concept introduction:
The absolute configuration of a molecule is a spatial arrangement of atoms. It is represented by two terms
(b)
Interpretation:
The reason as to why
Concept introduction:
The absolute configuration of a molecule is a spatial arrangement of atoms. It is represented by two terms
Want to see the full answer?
Check out a sample textbook solutionChapter 27 Solutions
Organic Chemistry
- Consider the following peptide : Phe – Glu – Ser – Met and Val – Trp – Cys – Leu. Do these peptides have different net charges at (a) pH 1? (b) pH 7? Indicate the charges at both pH valuesarrow_forwardAn enzyme catalyzes the hydrolysis of an ester with a certain activity, but this activity is lost in a 3 M urea solution. What is the most likely explanation for the loss of activity? (A) Urea binds to the active site of the enzyme competitively with the substrate. (B) Urea causes the cleavage of the peptide bonds in the enzyme. (C) Urea causes the enzyme to denature and lose its specific three-dimensional shape. (D) Urea reacts with disulfide bonds in the enzyme.arrow_forward27. Which of the following statements about cholesterol is not correct? CH3 CH3 H. d но Cholesterol (a) Cholesterol is a steroid that contains a tetracyclic ring system. (b) Cholesterol is a steroid that contains 8 chiral carbons and can form 28 or 256 stereoisomers. (c) Each atom or group attached to a ring-junction carbon (i.e., carbons a -e) is in a trans or axial position. Because of this the tetracyclic ring system is mostly flat. (d) Cholesterol is used to synthesized vitamin D, bile acids, sex hormones, and adrenocorticoid hormones. (e) Cholesterol is not found in the cell membranes of animals.arrow_forward
- H. H. H. CH2 (CH2)4 NH3* CH2 но CH CH, CH CH2 CH2 H. (a) (b) (e) Which of the interactions stabilizing protein tertiary structure is (a)? O hydrophobic interaction O disulphide bridge bonding O hydrogen bonding O salt bridge bondingarrow_forwardWhat is the anhydride for each of the following acids:(a) H2SO4, (b) HClO3, (c) HNO2, (d) H2CO3, (e) H3PO4?arrow_forwardThe amino acid threonine has two chiral centers. The stereoisomer found in proteins has the configuration 2S,3R about the two chiral centers. Draw (a) a Fischer projection of this stereoisomer and (b) a three-dimensional representationarrow_forward
- Given that C6H11COOH has a pKa = 4.8 and C6H11N + H3 has a pKa = 10.7, what pH would you make the water layer to cause both compounds to dissolve in it?arrow_forwardQ1)In the pH range 1.82 to 8.99, H2Arg+ is the principal form of arginine. Which is the second most prominent species at pH 6.0? At pH 5.0?Q2) (a) Draw the structure of the predominant form (principal species) of 1,3-dihydroxybenzene at pH 9.00 and at pH 11.00.(b) What is the second most prominent species at each pH?(c) Calculate the percentage in the major form at each pHarrow_forward8. The following proteins represent a wide range of molecular weights and isoelectric points. Mr is the molecular weight of a single protein chain. • Protein 1: Mr 68,544; pl 6.11 (monomer) • Protein 2: Mr 29,041; pl 5.32 (dimer) • Protein 3: Mr 15,805; pl 5.7 (dimer) • Protein 4: Mr 12,165; pl 4.74 a. Which protein is the most acidic? Explain your answer. b. Which protein will migrate the slowest in an SDS-PAGE? Explain your answer. c. In what order will these proteins elute from a cation exchanger at pH 8? Explain your answer. d. In what order will these proteins salt out from a pH 7 solution by the dropwise addition of saturated ammonium sulfate? Explain your answer. 5 83°F Cloudyarrow_forward
- The activity of an enzyme requires a glutamic acid to display its -COOH functional group in the protonated state. Suppose the pK, of the -COOH group is 4.07. (a) Will the enzyme be more active at pH 3.5 or 4.5? Explain. (b) What fraction of the enzymes will be active at pH = 4.07? Explain. (c) At what pH will the enzyme show 78% of maximal activity?arrow_forward11. The structures of three amino acids are given below : NH2 0 Но -CH,CH-C-OH HOOCCH2CH2CH(NH2)COOH (1) (II)arrow_forwardExplain what is meant by the following :(i) peptide linkage(ii) pyranose structure of glucosearrow_forward
- Chemistry & Chemical ReactivityChemistryISBN:9781133949640Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage LearningChemistry & Chemical ReactivityChemistryISBN:9781337399074Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage LearningChemistry: Principles and PracticeChemistryISBN:9780534420123Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward MercerPublisher:Cengage Learning
- Introduction to General, Organic and BiochemistryChemistryISBN:9781285869759Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar TorresPublisher:Cengage Learning