Chemistry 2012 Student Edition (hard Cover) Grade 11
12th Edition
ISBN: 9780132525763
Author: Prentice Hall
Publisher: Prentice Hall
expand_more
expand_more
format_list_bulleted
Question
Chapter 24, Problem 67A
Interpretation Introduction
Interpretation: From the given pairs A-A, A-T, C-G, G-A, A-U, and T-U, the base pair found in the DNA molecule has to be identified.
Concept introduction:
Expert Solution & Answer
Answer to Problem 67A
A-T and C-G are base pairs found in the DNA molecule.
Explanation of Solution
Adenine (A), cytosine (C), guanine (G), and thymine (T) are the four nitrogen-containing base pairs that make up a DNA molecule. The bases adenine and thymine and cytosine and guanine form complementary pairs. In ribonucleic acid (RNA), uracil (U) replaces thymine, which is not present in DNA. The structure of DNA is formed by the pairing and binding of these base pairs.
The given pairs are A-A, A-T, C-G, G-A, A-U, and T-U.
Only A-T and C-G are base pairs found in DNA from the given pairs.
Conclusion
A-T and C-G are base pairs found in the DNA molecule.
Chapter 24 Solutions
Chemistry 2012 Student Edition (hard Cover) Grade 11
Ch. 24.1 - Prob. 1LCCh. 24.1 - Prob. 2LCCh. 24.1 - Prob. 3LCCh. 24.1 - Prob. 4LCCh. 24.1 - Prob. 5LCCh. 24.1 - Prob. 6LCCh. 24.1 - Prob. 7LCCh. 24.2 - Prob. 8LCCh. 24.2 - Prob. 9LCCh. 24.2 - Prob. 10LC
Ch. 24.2 - Prob. 11LCCh. 24.2 - Prob. 12LCCh. 24.2 - Prob. 13LCCh. 24.2 - Prob. 14LCCh. 24.2 - Prob. 15LCCh. 24.3 - Prob. 16LCCh. 24.3 - Prob. 17LCCh. 24.3 - Prob. 18LCCh. 24.3 - Prob. 19LCCh. 24.3 - Prob. 20LCCh. 24.3 - Prob. 21LCCh. 24.4 - Prob. 22LCCh. 24.4 - Prob. 23LCCh. 24.4 - Prob. 24LCCh. 24.4 - Prob. 25LCCh. 24.4 - Prob. 26LCCh. 24.4 - Prob. 27LCCh. 24.4 - Prob. 28LCCh. 24.5 - Prob. 29LCCh. 24.5 - Prob. 30LCCh. 24.5 - Prob. 31LCCh. 24.5 - Prob. 32LCCh. 24.5 - Prob. 33LCCh. 24.6 - Prob. 35LCCh. 24.6 - Prob. 36LCCh. 24.6 - Prob. 37LCCh. 24.6 - Prob. 38LCCh. 24.6 - Prob. 39LCCh. 24.6 - Prob. 40LCCh. 24 - Prob. 41ACh. 24 - Prob. 42ACh. 24 - Prob. 43ACh. 24 - Prob. 44ACh. 24 - Prob. 45ACh. 24 - Prob. 46ACh. 24 - Prob. 47ACh. 24 - Prob. 48ACh. 24 - Prob. 49ACh. 24 - Prob. 50ACh. 24 - Prob. 51ACh. 24 - Prob. 52ACh. 24 - Prob. 53ACh. 24 - Prob. 54ACh. 24 - Prob. 55ACh. 24 - Prob. 56ACh. 24 - Prob. 57ACh. 24 - Prob. 58ACh. 24 - Prob. 59ACh. 24 - Prob. 60ACh. 24 - Prob. 61ACh. 24 - Prob. 62ACh. 24 - Prob. 63ACh. 24 - Prob. 64ACh. 24 - Prob. 65ACh. 24 - Prob. 66ACh. 24 - Prob. 67ACh. 24 - Prob. 68ACh. 24 - Prob. 69ACh. 24 - Prob. 70ACh. 24 - Prob. 71ACh. 24 - Prob. 72ACh. 24 - Prob. 73ACh. 24 - Prob. 74ACh. 24 - Prob. 75ACh. 24 - Prob. 76ACh. 24 - Prob. 77ACh. 24 - Prob. 78ACh. 24 - Prob. 79ACh. 24 - Prob. 80ACh. 24 - Prob. 81ACh. 24 - Prob. 82ACh. 24 - Prob. 83ACh. 24 - Prob. 84ACh. 24 - Prob. 85ACh. 24 - Prob. 86ACh. 24 - Prob. 87ACh. 24 - Prob. 88ACh. 24 - Prob. 89ACh. 24 - Prob. 90ACh. 24 - Prob. 91ACh. 24 - Prob. 92ACh. 24 - Prob. 93ACh. 24 - Prob. 94ACh. 24 - Prob. 95ACh. 24 - Prob. 96ACh. 24 - Prob. 97ACh. 24 - Prob. 98ACh. 24 - Prob. 99ACh. 24 - Prob. 100ACh. 24 - Prob. 101ACh. 24 - Prob. 102ACh. 24 - Prob. 103ACh. 24 - Prob. 104ACh. 24 - Prob. 105ACh. 24 - Prob. 106ACh. 24 - Prob. 107ACh. 24 - Prob. 108ACh. 24 - Prob. 109ACh. 24 - Prob. 110ACh. 24 - Prob. 111ACh. 24 - Prob. 112ACh. 24 - Prob. 113ACh. 24 - Prob. 115ACh. 24 - Prob. 116ACh. 24 - Prob. 117ACh. 24 - Prob. 118ACh. 24 - Prob. 119ACh. 24 - Prob. 120ACh. 24 - Prob. 121ACh. 24 - Prob. 122ACh. 24 - Prob. 123ACh. 24 - Prob. 124ACh. 24 - Prob. 125ACh. 24 - Prob. 126ACh. 24 - Prob. 127ACh. 24 - Prob. 128ACh. 24 - Prob. 129ACh. 24 - Prob. 130ACh. 24 - Prob. 131ACh. 24 - Prob. 132ACh. 24 - Prob. 133ACh. 24 - Prob. 1STPCh. 24 - Prob. 2STPCh. 24 - Prob. 3STPCh. 24 - Prob. 4STPCh. 24 - Prob. 5STPCh. 24 - Prob. 6STPCh. 24 - Prob. 7STPCh. 24 - Prob. 8STPCh. 24 - Prob. 9STPCh. 24 - Prob. 10STPCh. 24 - Prob. 11STPCh. 24 - Prob. 12STPCh. 24 - Prob. 13STPCh. 24 - Prob. 14STP
Knowledge Booster
Similar questions
- Q2: Ranking Acidity a) Rank the labeled protons in the following molecule in order of increasing pKa. Briefly explain the ranking. Use Table 2.2 as reference. Ha Нь HC H-N Ha OHe b) Atenolol is a drug used to treat high blood pressure. Which of the indicated N-H bonds is more acidic? Explain. (Hint: use resonance structures to help) Name the functional groups on atenolol. H H-N atenolol Ν H-N OH Нarrow_forwardAnswer d, e, and farrow_forwardIf the rotational constant of a molecule is B = 120 cm-1, it can be stated that the transition from 2←1:a) gives rise to a line at 120 cm-1b) is a forbidden transitionc) gives rise to a line at 240 cm-1d) gives rise to a line at 480 cm-1arrow_forward
- Briefly indicate the coordination forms of B and Si in borates and silicates, respectively.arrow_forwardCan you please draw out the Lewis structure for these two formulasarrow_forwardIn a rotational Raman spectrum of a diatomic molecule it is correct to say that:a) anti-Stokes lines occur at frequencies higher than the excitatory oneb) Stokes lines occur at frequencies higher than the excitatory onec) Rayleigh scattering is not observedd) Rayleigh scattering corresponds to delta J = 0arrow_forward
- Of the molecules: H2, N2, HCl, CO2, indicate which ones can give Raman vibration-rotation spectra:a) H2, N2 and HClb) H2, N2, HCl and CO2c) H2 and N2d) all of themarrow_forwardCan you please help me with drawing the Lewis structure of each molecular formula?I truly appreciate you!arrow_forwardCan you please help me with drawing the Lewis structure of each molecular formula?I truly appreciate you!arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage Learning
ChemistryChemistryISBN:9781259911156Author:Raymond Chang Dr., Jason Overby ProfessorPublisher:McGraw-Hill Education
Principles of Instrumental AnalysisChemistryISBN:9781305577213Author:Douglas A. Skoog, F. James Holler, Stanley R. CrouchPublisher:Cengage Learning
Organic ChemistryChemistryISBN:9780078021558Author:Janice Gorzynski Smith Dr.Publisher:McGraw-Hill Education
Chemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage Learning
Elementary Principles of Chemical Processes, Bind...ChemistryISBN:9781118431221Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. BullardPublisher:WILEY
Chemistry
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning
Chemistry
Chemistry
ISBN:9781259911156
Author:Raymond Chang Dr., Jason Overby Professor
Publisher:McGraw-Hill Education
Principles of Instrumental Analysis
Chemistry
ISBN:9781305577213
Author:Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:Cengage Learning
Organic Chemistry
Chemistry
ISBN:9780078021558
Author:Janice Gorzynski Smith Dr.
Publisher:McGraw-Hill Education
Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
Publisher:Cengage Learning
Elementary Principles of Chemical Processes, Bind...
Chemistry
ISBN:9781118431221
Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:WILEY