Essential Organic Chemistry Study Guide & Solution Manual, Books a la Carte Edition
3rd Edition
ISBN: 9780134255644
Author: Bruice, Paula Yurkanis
Publisher: PEARSON
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Textbook Question
Chapter 21.9, Problem 11P
List the possible codons on mRNA that specify each amino acid in Problem 6 and the anticodon on the tRNA that carries that amino acid.
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Chapter 21 Solutions
Essential Organic Chemistry Study Guide & Solution Manual, Books a la Carte Edition
Ch. 21.1 - Draw the structure for each of the following: a....Ch. 21.3 - If one of the strands of DNA has the following...Ch. 21.4 - The 2,3-cyclic phosphodiester that is formed...Ch. 21.5 - Using a dark line for the original parental DNA...Ch. 21.7 - Why do both thymine and uracil specify the...Ch. 21.9 - If methionine is always the first amino acid...Ch. 21.9 - Four Cs occur in a row in the segment of mRNA...Ch. 21.9 - UAA is a stop codon. Why does the UAA sequence in...Ch. 21.9 - A change in which base of a codon would be least...Ch. 21.9 - Write the sequences of bases in the sense strand...
Ch. 21.9 - List the possible codons on mRNA that specify each...Ch. 21.10 - Adenine can be deaminated to hypoxanthine, and...Ch. 21.10 - Explain why thymine cannot be deaminated.Ch. 21.12 - Which of the following base sequences would most...Ch. 21 - Draw structures for the following: a....Ch. 21 - What nonapeptide is coded for by the following...Ch. 21 - What is the sequence of bases in the template...Ch. 21 - What is the sequence of bases in the sense strand...Ch. 21 - What would be the C-terminal amino acid if the...Ch. 21 - What would be the base sequence of the segment of...Ch. 21 - Propose a mechanism for the following reaction:Ch. 21 - A segment of DNA has 18 base pairs. It has 7...Ch. 21 - Match the codon with the anticodon: Codon: AAA GCA...Ch. 21 - Using the single-letter abbreviations for the...Ch. 21 - Indicate whether each functional group of the five...Ch. 21 - Using the A and D designations in Problem 25,...Ch. 21 - Which of the following pairs of dinucleotides are...Ch. 21 - If an mRNA contained only U and G in random...Ch. 21 - Why is the codon a triplet rather than a doublet...Ch. 21 - Human immunodeficiency virus (HIV) is the...Ch. 21 - The amino acid sequences of peptide fragments...Ch. 21 - Which cytosine in the following sense strand of...Ch. 21 - Prob. 33PCh. 21 - Why does DNA not unravel completely before...Ch. 21 - The first amino acid incorporated into a...
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- Use the References to access important values if needed for this question. What is the IUPAC name of each of the the following? 0 CH3CHCNH₂ CH3 CH3CHCNHCH2CH3 CH3arrow_forwardYou have now performed a liquid-liquid extraction protocol in Experiment 4. In doing so, you manipulated and exploited the acid-base chemistry of one or more of the compounds in your mixture to facilitate their separation into different phases. The key to understanding how liquid- liquid extractions work is by knowing which layer a compound is in, and in what protonation state. The following liquid-liquid extraction is different from the one you performed in Experiment 4, but it uses the same type of logic. Your task is to show how to separate apart Compound A and Compound B. . Complete the following flowchart of a liquid-liquid extraction. Handwritten work is encouraged. • Draw by hand (neatly) only the appropriate organic compound(s) in the boxes. . Specify the reagent(s)/chemicals (name is fine) and concentration as required in Boxes 4 and 5. • Box 7a requires the solvent (name is fine). • Box 7b requires one inorganic compound. • You can neatly complete this assignment by hand and…arrow_forwardb) Elucidate compound D w) mt at 170 nd shows c-1 stretch at 550cm;' The compound has the ff electronic transitions: 0%o* and no a* 1H NMR Spectrum (CDCl3, 400 MHz) 3.5 3.0 2.5 2.0 1.5 1.0 0.5 ppm 13C{H} NMR Spectrum (CDCl3, 100 MHz) Solvent 80 70 60 50 40 30 20 10 0 ppm ppm ¹H-13C me-HSQC Spectrum ppm (CDCl3, 400 MHz) 5 ¹H-¹H COSY Spectrum (CDCl3, 400 MHz) 0.5 10 3.5 3.0 2.5 2.0 1.5 1.0 10 15 20 20 25 30 30 -35 -1.0 1.5 -2.0 -2.5 3.0 -3.5 0.5 ppm 3.5 3.0 2.5 2.0 1.5 1.0 0.5 ppmarrow_forward
- Part I. a) Elucidate the structure of compound A using the following information. • mass spectrum: m+ = 102, m/2=57 312=29 • IR spectrum: 1002.5 % TRANSMITTANCE Ngg 50 40 30 20 90 80 70 60 MICRONS 5 8 9 10 12 13 14 15 16 19 1740 cm M 10 0 4000 3600 3200 2800 2400 2000 1800 1600 13 • CNMR 'H -NMR Peak 8 ppm (H) Integration multiplicity a 1.5 (3H) triplet b 1.3 1.5 (3H) triplet C 2.3 1 (2H) quartet d 4.1 1 (2H) quartet & ppm (c) 10 15 28 60 177 (C=0) b) Elucidate the structure of compound B using the following information 13C/DEPT NMR 150.9 MHz IIL 1400 WAVENUMBERS (CM-1) DEPT-90 DEPT-135 85 80 75 70 65 60 55 50 45 40 35 30 25 20 ppm 1200 1000 800 600 400arrow_forward• Part II. a) Elucidate The structure of compound c w/ molecular formula C10 11202 and the following data below: • IR spectra % TRANSMITTANCE 1002.5 90 80 70 60 50 40 30 20 10 0 4000 3600 3200 2800 2400 2000 1800 1600 • Information from 'HAMR MICRONS 8 9 10 11 14 15 16 19 25 1400 WAVENUMBERS (CM-1) 1200 1000 800 600 400 peak 8 ppm Integration multiplicity a 2.1 1.5 (3H) Singlet b 3.6 1 (2H) singlet с 3.8 1.5 (3H) Singlet d 6.8 1(2H) doublet 7.1 1(2H) doublet Information from 13C-nmR Normal carbon 29ppm Dept 135 Dept -90 + NO peak NO peak 50 ppm 55 ppm + NO peak 114 ppm t 126 ppm No peak NO peak 130 ppm t + 159 ppm No peak NO peak 207 ppm по реак NO peakarrow_forwardCould you redraw these and also explain how to solve them for me pleasarrow_forward
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