Essential Organic Chemistry (3rd Edition)
3rd Edition
ISBN: 9780321937711
Author: Paula Yurkanis Bruice
Publisher: PEARSON
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Chapter 21.7, Problem 5P
Why do both thymine and uracil specify the incorporation of adenine?
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Highlight each glycosidic bond in the molecule below. Then answer the questions in the table under the drawing area.
HO-
HO-
-0
OH
OH
HO
NG
HO-
HO-
OH
OH
OH
OH
NG
OH
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+
Suppose the molecule in the drawing area below were reacted with H₂ over a platinum catalyst. Edit the molecule to show what would happen to it. That is, turn
it into the product of the reaction.
Also, write the name of the product molecule under the drawing area.
Name: ☐
H
C=0
X
H-
OH
HO-
H
HO-
-H
CH₂OH
×
Draw the Haworth projection of the disaccharide made by joining D-glucose and D-mannose with a ẞ(1-4) glycosidic bond. If the disaccharide has more than
one anomer, you can draw any of them.
Click and drag to start drawing a
structure.
X
Chapter 21 Solutions
Essential Organic Chemistry (3rd 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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- Epoxides can be opened in aqueous acid or aqueous base to produce diols (molecules with two OH groups). In this question, you'll explore the mechanism of epoxide opening in aqueous acid. 2nd attempt Be sure to show all four bonds at stereocenters using hash and wedge lines. 0 0 Draw curved arrows to show how the epoxide reacts with hydronium ion. 100 +1: 1st attempt Feedback Be sure to show all four bonds at stereocenters using hash and wedge lines. See Periodic Table See Hint H A 5 F F Hr See Periodic Table See Hintarrow_forward03 Question (1 point) For the reaction below, draw both of the major organic products. Be sure to consider stereochemistry. > 1. CH₂CH₂MgBr 2. H₂O 3rd attempt Draw all four bonds at chiral centers. Draw all stereoisomers formed. Draw the structures here. e 130 AN H See Periodic Table See Hint P C Brarrow_forwardYou may wish to address the following issues in your response if they are pertinent to the reaction(s) you propose to employ:1) Chemoselectivity (why this functional group and not another?) 2) Regioselectivity (why here and not there?) 3) Stereoselectivity (why this stereoisomer?) 4) Changes in oxidation state. Please make it in detail and draw it out too in what step what happens. Thank you for helping me!arrow_forward
- 1) Chemoselectivity (why this functional group and not another?) 2) Regioselectivity (why here and not there?) 3) Stereoselectivity (why this stereoisomer?) 4) Changes in oxidation state. Everything in detail and draw out and write it.arrow_forwardCalculating the pH at equivalence of a titration 3/5 Izabella A chemist titrates 120.0 mL of a 0.7191M dimethylamine ((CH3)2NH) solution with 0.5501 M HBr solution at 25 °C. Calculate the pH at equivalence. The pk of dimethylamine is 3.27. Round your answer to 2 decimal places. Note for advanced students: you may assume the total volume of the solution equals the initial volume plus the volume of HBr solution added. pH = ☐ ✓ 18 Ar Boarrow_forwardAlcohols can be synthesized using an acid-catalyzed hydration of an alkene. An alkene is combined with aqueous acid (e.. sulfuric acid in water). The reaction mechanism typically involves a carbocation intermediate. > 3rd attempt 3343 10 8 Draw arrows to show the reaction between the alkene and hydronium ion. that 2nd attempt Feedback 1st attempt تعمال Ju See Periodic Table See Hint F D Ju See Periodic Table See Hintarrow_forward
- Draw the simplified curved arrow mechanism for the reaction of acetone and CHgLi to give the major product. 4th attempt Π Draw the simplified curved arrow mechanism T 3rd attempt Feedback Ju See Periodic Table See Hint H -H H -I H F See Periodic Table See Hintarrow_forwardSelect the correct reagent to accomplish the first step of this reaction. Then draw a mechanism on the Grignard reagent using curved arrow notation to show how it is converted to the final product. 4th attempt Part 1 (0.5 point) Select the correct reagent to accomplish the first step of this reaction. Choose one: OA Mg in ethanol (EtOH) OB. 2 Li in THF O C. Li in THF D. Mg in THF O E Mg in H2O Part 2 (0.5 point) Br Part 1 Bri Mg CH B CH, 1 Draw intermediate here, but no arrows. © TE See Periodic Table See Hint See Hint ין Harrow_forwardSelect the product for the following reaction. HO HO PCC OH ○ OH O HO ○ HO HO HOarrow_forward
- 5:45 Х Select the final product for the following reaction sequence. O O 1. Mg. ether 2.D.Oarrow_forwardBased on the chart Two similarities between the molecule with alpha glycosidic linkages. Two similarities between the molecules with beta glycosidtic linkages. Two differences between the alpha and beta glycosidic linkages.arrow_forwardplease help fill in the tablearrow_forward
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