Introduction to General, Organic and Biochemistry
12th Edition
ISBN: 9780357391594
Author: Frederick A. Bettelheim; William H. Brown; Mary K. Campbell
Publisher: Cengage Learning US
expand_more
expand_more
format_list_bulleted
Question
Chapter 24, Problem 9P
Interpretation Introduction
Interpretation:
Interpret difference in structure between thymine and uracil.
Concept Introduction:
Four type of bases are present in DNA as well as in RNA. The nitrogenous bases may be adenine, guanine, cytosine or thymine while in DNA deoxyribose sugar is present and in RNA ribose sugar is present. In RNA, uracil is present as base in place of thymine.
Expert Solution & Answer

Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
Using the table of Reactants and Products provided in the Hints section, provide the major product
(with the correct stereochemistry when applicable) for questions below by selecting the letter that
corresponds to the exact chemical structures for the possible product.
OH conc Hydrochloric
acid
40°C Temp
A/
Using arrows to designate the flow of electrons, complete the reaction below and
provide a detailed mechanism for the formation of the product
OH
conc Hydrochloric
acid
40°C Temp
All chemical structures should be hand drawn on a piece of paper
Paragraph
BI UAE +v
draw out the following structures plese
Chapter 24 Solutions
Introduction to General, Organic and Biochemistry
Ch. 24.2 - Problem 25-1 Draw the structure of UMP.Ch. 24.3 - Prob. 24.2QCCh. 24.3 - Prob. 24.3QCCh. 24.4 - Prob. 24.4QCCh. 24.5 - Prob. 24.5QCCh. 24.6 - Prob. 24.6QCCh. 24.7 - Prob. 24.7QCCh. 24.8 - Prob. 24.8QCCh. 24 - Prob. 1PCh. 24 - 25-2 What structures Of the cell, visible in a...
Ch. 24 - 25-3 Name one hereditary disease.Ch. 24 - 25-4 What is the basis unit of heredity?Ch. 24 - 25-5 (a) Where in a cell is the DNA located? (b)...Ch. 24 - 25-6 What are the components of (a) a nucleotide...Ch. 24 - 25-7 What are the differences between DNA and RNA?Ch. 24 - 25-8 Draw the structures of ADP and GDP. Are these...Ch. 24 - Prob. 9PCh. 24 - 25-10 Which DNA and RNA bases contain a carbonyl...Ch. 24 - Prob. 11PCh. 24 - Prob. 12PCh. 24 - Prob. 13PCh. 24 - Prob. 14PCh. 24 - Prob. 15PCh. 24 - Prob. 16PCh. 24 - Prob. 17PCh. 24 - 25-18 What type of bond connects the base to the...Ch. 24 - Prob. 19PCh. 24 - 25-20 What constitutes the backbone of DNA?Ch. 24 - Prob. 21PCh. 24 - 25-22 In DNA, which carbon atoms of...Ch. 24 - 25-23 The sequence Of a short DNA segment is...Ch. 24 - Prob. 24PCh. 24 - Prob. 25PCh. 24 - Prob. 26PCh. 24 - Prob. 27PCh. 24 - Prob. 28PCh. 24 - 25-29 What constitutes the superstructure of...Ch. 24 - 25-30 What is the primary structure of DNA?Ch. 24 - 25-31 What is the secondary structure of DNA?Ch. 24 - 25-32 What is the major groove of a DNA helix?Ch. 24 - 25-33 What are the higher-order structures of DNA...Ch. 24 - 25-34 Which type Of RNA has enzyme activity? Where...Ch. 24 - 25-35 Which has the longest chains: tRNA, mRNA, or...Ch. 24 - 25-36 Which type of RNA contains modified...Ch. 24 - 25-37 Which type Of RNA has a sequence exactly...Ch. 24 - 25-38 Where is rRNA located in the cell?Ch. 24 - Prob. 39PCh. 24 - Prob. 40PCh. 24 - Prob. 41PCh. 24 - Prob. 42PCh. 24 - Prob. 43PCh. 24 - 25-50 Define: (a) Intron (b) ExonCh. 24 - 25-51 Does mRNA also have introns and exons?...Ch. 24 - Prob. 46PCh. 24 - Prob. 47PCh. 24 - 25-54 Do all genes code for a protein? If not,...Ch. 24 - Prob. 49PCh. 24 - Prob. 50PCh. 24 - Prob. 51PCh. 24 - Prob. 52PCh. 24 - Prob. 53PCh. 24 - Prob. 54PCh. 24 - Prob. 55PCh. 24 - Prob. 56PCh. 24 - 25-55 A DNA molecule normally replicates itself...Ch. 24 - 25-56 Which functional groups on the bases form...Ch. 24 - Prob. 59PCh. 24 - 25-58 Draw the structures of cytosine and guanine...Ch. 24 - 25-59 How many different bases are present in a...Ch. 24 - Prob. 62PCh. 24 - 25-61 Why is replication called semiconservative?Ch. 24 - 25-62 How does the removal of some positive...Ch. 24 - 25-63 Write the chemical reaction for the...Ch. 24 - Prob. 66PCh. 24 - 25-65 What are helicases? What is their function?Ch. 24 - 25-66 Can dATP Serve as a source for a primer?Ch. 24 - Prob. 69PCh. 24 - Prob. 70PCh. 24 - 25-69 In which direction is the DNA molecule...Ch. 24 - Prob. 72PCh. 24 - Prob. 73PCh. 24 - Prob. 74PCh. 24 - 25-73 From the perspective of the chain being...Ch. 24 - Prob. 76PCh. 24 - Prob. 77PCh. 24 - Prob. 78PCh. 24 - Prob. 79PCh. 24 - Prob. 80PCh. 24 - Prob. 81PCh. 24 - Prob. 82PCh. 24 - Prob. 83PCh. 24 - Prob. 84PCh. 24 - Prob. 85PCh. 24 - Prob. 86PCh. 24 - Prob. 87PCh. 24 - Prob. 88PCh. 24 - Prob. 89PCh. 24 - Prob. 90PCh. 24 - Prob. 91PCh. 24 - Prob. 92PCh. 24 - Prob. 93PCh. 24 - (Chemical Connections 24E) What gene associated...Ch. 24 - Prob. 95PCh. 24 - -104 Why is it important that a DNA molecule be...Ch. 24 - Prob. 97PCh. 24 - Prob. 98PCh. 24 - Prob. 99PCh. 24 - Prob. 100PCh. 24 - -109 In sheep DNA, the mol% of adenine (A) was...Ch. 24 - Prob. 102PCh. 24 - Prob. 103PCh. 24 - Prob. 104PCh. 24 - Prob. 105PCh. 24 - -114 How could life have evolved if DNA leads to...Ch. 24 - Prob. 107PCh. 24 - Prob. 108PCh. 24 - Prob. 109P
Knowledge Booster
Similar questions
- Draw everything on a piece of paper outlining the synthesis from acetaldehyde to 2 cyclopentene carboxaldehyde using carbon based reagants with 3 carbons or fewers. Here is the attached image.arrow_forwardManoharan Mariappan, FR.D., 34) Complete the following reaction starting from hex-1-yne proceeding via different substitution reactions forming 2-heptanone. (25 pts). A Sia₂BH H₂O₂ NaOH Br D Mechanism for reaction D - ether-cleavage: 10 B Ph-MgCI, THF H₁₂O+ D HBr (XS) C TsCl, Py CH3-CH2-CH2-ONaarrow_forwardIn the table below, the correct structure for (2R)-3-methylpentan-2-ol (IUPAC name) can be represented by the letter OH OH HE > ' ÕH C B OH D A/ E OHarrow_forward
- Predict the major products of the following organic reaction: + A Δ ? Some important notes: • Draw the major product, or products, of the reaction in the drawing area below. • If there aren't any products, because no reaction will take place, check the box below the drawing area instead. Be sure to use wedge and dash bonds when necessary, for example to distinguish between major products that are enantiomers. Check Click and drag to start drawing a structure. Save For Later 2025 McGraw Hill LLC. All Rights Reserved. Terms of Usearrow_forwardWhy is analysing salt content (using Mohr titration) in both regular & salt reduced tomato sauce important?arrow_forwardIn the image below, correctly name the glassware # _P ( Blank 1) and T ( Blank 2). 景 A W Blank # 1 Blank #2 1000 +19 E E D 0 0-0 G H A A K Π 12 R M N S 0-0-arrow_forward
- Feedback: Your answer is incorrect. Predict the major products of the following organic reaction: CN Δ + A ? NC Some important notes: • Draw the major product, or products, of the reaction in the drawing area below. • If there aren't any products, because no reaction will take place, check the box below the drawing area instead. • Be sure to use wedge and dash bonds when necessary, for example to distinguish between major products that are enantiomers. esc Check 80 MH F1 F2 F3 F4 F5 50 @ # C % 95 € Save For Later Sub 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy C A DII F6 F7 F8 7 * 8 Λ & 6 F9 F10 9 0 4arrow_forwardIncorrect Feedback: Your answer is incorrect. Predict the major products of the following organic reaction: ཤིགས་བྱ རྩ་ཅད་ཀྱིས་༢༩ + Some important notes: A ^ ? • Draw the major product, or products, of the reaction in the drawing area below. • If there aren't any products, because no reaction will take place, check the box below the drawing area instead. • Be sure to use wedge and dash bonds when necessary, for example to distinguish between major products that are enantiomers. E Check 0 لا Save For La ©2025 McGraw Hill LLC. All Rights Reserved. Terms of All F9 Aarrow_forwardPredict the major products of the following organic reaction: + Δ A ? Some important notes: • Draw the major product, or products, of the reaction in the drawing area below. • If there aren't any products, because no reaction will take place, check the box below the drawing area instead. • Be sure to use wedge and dash bonds when necessary, for example to distinguish between major products that are enantiomers. Explanation Check Click and drag to start drawing a structure. 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use Privaarrow_forward
- esc 2 Incorrect Feedback: Your answer is incorrect. Can the molecule on the right-hand side of this organic reaction be made in good yield from no more than two reactants, in one step, by moderately heating the reactants? ? A O • If your answer is yes, then draw the reactant or reactants in the drawing area below. You can draw the reactants in any arrangement you like. . If your answer is no, check the box under the drawing area instead. Check F1 ! @ X C Save For Later Submit Assignment 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessibility 80 et A ད 1 4 F2 F3 F4 F5 F6 F7 F8 F9 F10 F11 F12 # $ 45 % A 6 87 & * 8 9 ) 0 + ||arrow_forwardCan the molecule on the right-hand side of this organic reaction be made in good yield from no more than two reactants, in one step, by moderately heating the reactants? ?A Δ O • If your answer is yes, then draw the reactant or reactants in the drawing area below. You can draw the reactants in any arrangement you like. • If your answer is no, check the box under the drawing area instead. Explanation Check Click and drag to start drawing a structure. 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessibilit ku F11arrow_forward१ eq ine teaching and × + rn/takeAssignment/takeCovalentActivity.do?locator-assignment-take [Review Topics] [References] Write an acceptable IUPAC name for the compound below. (Only systematic names, not common names are accepted by this question.) Keep the information page open for feedback reference. The IUPAC name is In progress mit Answer Retry Entire Group 5 more group attempts remaining Cengage Learning | Cengage Technical Support Save and Exitarrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- Introduction to General, Organic and BiochemistryChemistryISBN:9781285869759Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar TorresPublisher:Cengage LearningIntroductory Chemistry: A FoundationChemistryISBN:9781337399425Author:Steven S. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage Learning
- World of Chemistry, 3rd editionChemistryISBN:9781133109655Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCostePublisher:Brooks / Cole / Cengage Learning

Introduction to General, Organic and Biochemistry
Chemistry
ISBN:9781285869759
Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar Torres
Publisher:Cengage Learning

Introductory Chemistry: A Foundation
Chemistry
ISBN:9781337399425
Author:Steven S. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning

Chemistry for Today: General, Organic, and Bioche...
Chemistry
ISBN:9781305960060
Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen
Publisher:Cengage Learning

World of Chemistry, 3rd edition
Chemistry
ISBN:9781133109655
Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCoste
Publisher:Brooks / Cole / Cengage Learning