Introduction to General, Organic and Biochemistry
12th Edition
ISBN: 9780357119303
Author: Bettelheim, Frederick A., Brown, William H., Campbell, Mary K., FARRELL, Shawn O., Torres, Omar
Publisher: Cengage Learning
expand_more
expand_more
format_list_bulleted
Concept explainers
Videos
Question
Chapter 30, Problem 26P
Interpretation Introduction
Interpretation:
The creation of a new protein on the variable portion of a heavy chain by V(J)D recombination should be explained.
Concept Introduction:
The molecule of an immunoglobulin exhibits two polypeptide chains and two heavy polypeptide chains. These chains possess variable and constant regions. The constant regions exhibit a similar sequence of amino acids in different antibodies, and the variable regions exhibit a distinct sequence of amino acids in different antibodies.
Expert Solution & Answer
Trending nowThis is a popular solution!
Students have asked these similar questions
13. (11pts total) Consider the arrows pointing at three different carbon-carbon bonds in the
molecule depicted below.
Bond B
2°C. +2°C. cleavage
Bond A
•CH3 + 26.← Cleavage
2°C. +
Bond C
+3°C•
CH3 2C
Cleavage
E
2°C. 26.
weakest bond
Intact molecule
Strongest 3°C 20.
Gund
Largest
argest
a. (2pts) Which bond between A-C is weakest? Which is strongest? Place answers in
appropriate boxes.
C
Weakest
bond
A
Produces
Most
Bond
Strongest
Bond
Strongest Gund
produces least stable
radicals
Weakest
Stable radical
b. (4pts) Consider the relative stability of all cleavage products that form when bonds A,
B, AND C are homolytically cleaved/broken. Hint: cleavage products of bonds A, B,
and C are all carbon radicals.
i. Which ONE cleavage product is the most stable? A condensed or bond line
representation is fine.
13°C. formed in
bound C
cleavage
ii. Which ONE cleavage product is the least stable? A condensed or bond line
representation is fine.
• CH3
methyl radical
Formed in Gund A Cleavage
c.…
Br.
COOH Br,
FCH COOH E
FeBr
ASOCI
B
NH
(CH,CO),OD Br₂
2
C
alcKOH
Find A to F (all)
Chapter 30 Solutions
Introduction to General, Organic and Biochemistry
Ch. 30.1 - Prob. 30.1QCCh. 30.2 - Prob. 30.2QCCh. 30.3 - Prob. 30.3QCCh. 30.4 - Prob. 30.4QCCh. 30.5 - Prob. 30.5QCCh. 30.6 - Prob. 30.6QCCh. 30.7 - Prob. 30.7QCCh. 30.8 - Prob. 30.8QCCh. 30 - Give two examples of external innate immunity in...Ch. 30 - Prob. 2P
Ch. 30 - Prob. 3PCh. 30 - Prob. 4PCh. 30 - Prob. 5PCh. 30 - Prob. 6PCh. 30 - Prob. 7PCh. 30 - 31-8 What are memory cells? What is their...Ch. 30 - Prob. 9PCh. 30 - Prob. 10PCh. 30 - Prob. 11PCh. 30 - Prob. 12PCh. 30 - Prob. 13PCh. 30 - Prob. 14PCh. 30 - Prob. 15PCh. 30 - Prob. 16PCh. 30 - When a foreign substance is injected in a rabbit,...Ch. 30 - Prob. 18PCh. 30 - (a) Which immunoglobulin has the highest...Ch. 30 - Prob. 20PCh. 30 - Prob. 21PCh. 30 - Prob. 22PCh. 30 - Prob. 23PCh. 30 - Prob. 24PCh. 30 - Prob. 25PCh. 30 - Prob. 26PCh. 30 - What accounts for antibody diversity?Ch. 30 - Prob. 28PCh. 30 - Prob. 29PCh. 30 - Prob. 30PCh. 30 - Prob. 31PCh. 30 - Prob. 32PCh. 30 - Prob. 33PCh. 30 - Prob. 34PCh. 30 - Prob. 35PCh. 30 - Prob. 36PCh. 30 - Prob. 37PCh. 30 - Prob. 38PCh. 30 - Prob. 39PCh. 30 - Prob. 40PCh. 30 - Prob. 41PCh. 30 - Prob. 42PCh. 30 - Prob. 43PCh. 30 - Prob. 44PCh. 30 - Prob. 45PCh. 30 - Prob. 46PCh. 30 - Prob. 47PCh. 30 - Prob. 48PCh. 30 - Prob. 49PCh. 30 - Prob. 50PCh. 30 - Prob. 51PCh. 30 - Prob. 52PCh. 30 - Prob. 53PCh. 30 - Prob. 54PCh. 30 - Prob. 55PCh. 30 - Prob. 56PCh. 30 - Prob. 57PCh. 30 - Prob. 58PCh. 30 - Prob. 59PCh. 30 - Prob. 60PCh. 30 - Prob. 61PCh. 30 - Prob. 62PCh. 30 - Prob. 63PCh. 30 - Prob. 64PCh. 30 - Prob. 65PCh. 30 - Prob. 66PCh. 30 - Prob. 67PCh. 30 - Prob. 68PCh. 30 - Prob. 69PCh. 30 - Prob. 70PCh. 30 - How are researchers attempting to use gene therapy...Ch. 30 - Prob. 72PCh. 30 - (Chemical Connections 30A ) Why are monoclonal...Ch. 30 - Prob. 74PCh. 30 - Prob. 75PCh. 30 - Prob. 76PCh. 30 - Prob. 77PCh. 30 - Prob. 78PCh. 30 - Prob. 79PCh. 30 - Prob. 80PCh. 30 - Prob. 81PCh. 30 - Prob. 82PCh. 30 - Prob. 83PCh. 30 - Prob. 84PCh. 30 - Prob. 85PCh. 30 - Prob. 86PCh. 30 - Prob. 87PCh. 30 - Prob. 88PCh. 30 - Prob. 89PCh. 30 - Prob. 90PCh. 30 - Prob. 91PCh. 30 - Prob. 92PCh. 30 - Prob. 93PCh. 30 - Prob. 94PCh. 30 - Prob. 95PCh. 30 - Prob. 96PCh. 30 - Prob. 97PCh. 30 - Prob. 98PCh. 30 - Prob. 99PCh. 30 - Prob. 100PCh. 30 - Prob. 101PCh. 30 - Prob. 102PCh. 30 - Prob. 103PCh. 30 - Prob. 104P
Knowledge Booster
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.Similar questions
- Show work. don't give Ai generated solutionarrow_forwardHi!! Please provide a solution that is handwritten. Ensure all figures, reaction mechanisms (with arrows and lone pairs please!!), and structures are clearly drawn to illustrate the synthesis of the product as per the standards of a third year organic chemistry course. ****the solution must include all steps, mechanisms, and intermediate structures as required. Please hand-draw the mechanisms and structures to support your explanation. Don’t give me AI-generated diagrams or text-based explanations, no wordy explanations on how to draw the structures I need help with the exact mechanism hand drawn by you!!! I am reposting this—ensure all parts of the question are straightforward and clear or please let another expert handle it thanks!!arrow_forwardHi!! Please provide a solution that is handwritten. Ensure all figures, reaction mechanisms (with arrows and lone pairs please!!), and structures are clearly drawn to illustrate the synthesis of the product as per the standards of a third year organic chemistry course. ****the solution must include all steps, mechanisms, and intermediate structures as required. Please hand-draw the mechanisms and structures to support your explanation. Don’t give me AI-generated diagrams or text-based explanations, no wordy explanations on how to draw the structures I need help with the exact mechanism hand drawn by you!!! I am reposting this—ensure all parts of the question are straightforward and clear or please let another expert handle it thanks!!arrow_forward
- . (11pts total) Consider the arrows pointing at three different carbon-carbon bonds in the molecule depicted below. Bond B 2°C. +2°C. < cleavage Bond A • CH3 + 26. t cleavage 2°C• +3°C• Bond C Cleavage CH3 ZC '2°C. 26. E Strongest 3°C. 2C. Gund Largest BDE weakest bond In that molecule a. (2pts) Which bond between A-C is weakest? Which is strongest? Place answers in appropriate boxes. Weakest C bond Produces A Weakest Bond Most Strongest Bond Stable radical Strongest Gund produces least stable radicals b. (4pts) Consider the relative stability of all cleavage products that form when bonds A, B, AND C are homolytically cleaved/broken. Hint: cleavage products of bonds A, B, and C are all carbon radicals. i. Which ONE cleavage product is the most stable? A condensed or bond line representation is fine. 人 8°C. formed in bound C cleavage ii. Which ONE cleavage product is the least stable? A condensed or bond line representation is fine. methyl radical •CH3 formed in bund A Cleavagearrow_forwardWhich carbocation is more stable?arrow_forwardAre the products of the given reaction correct? Why or why not?arrow_forward
- The question below asks why the products shown are NOT the correct products. I asked this already, and the person explained why those are the correct products, as opposed to what we would think should be the correct products. That's the opposite of what the question was asking. Why are they not the correct products? A reaction mechanism for how we arrive at the correct products is requested ("using key intermediates"). In other words, why is HCl added to the terminal alkene rather than the internal alkene?arrow_forwardMy question is whether HI adds to both double bonds, and if it doesn't, why not?arrow_forwardStrain Energy for Alkanes Interaction / Compound kJ/mol kcal/mol H: H eclipsing 4.0 1.0 H: CH3 eclipsing 5.8 1.4 CH3 CH3 eclipsing 11.0 2.6 gauche butane 3.8 0.9 cyclopropane 115 27.5 cyclobutane 110 26.3 cyclopentane 26.0 6.2 cycloheptane 26.2 6.3 cyclooctane 40.5 9.7 (Calculate your answer to the nearest 0.1 energy unit, and be sure to specify units, kJ/mol or kcal/mol. The answer is case sensitive.) H. H Previous Nextarrow_forward
- A certain half-reaction has a standard reduction potential Ered +1.26 V. An engineer proposes using this half-reaction at the anode of a galvanic cell that must provide at least 1.10 V of electrical power. The cell will operate under standard conditions. Note for advanced students: assume the engineer requires this half-reaction to happen at the anode of the cell. Is there a minimum standard reduction potential that the half-reaction used at the cathode of this cell can have? If so, check the "yes" box and calculate the minimum. Round your answer to 2 decimal places. If there is no lower limit, check the "no" box.. Is there a maximum standard reduction potential that the half-reaction used at the cathode of this cell can have? If so, check the "yes" box and calculate the maximum. Round your answer to 2 decimal places. If there is no upper limit, check the "no" box. yes, there is a minimum. 1 red Πν no minimum Oyes, there is a maximum. 0 E red Dv By using the information in the ALEKS…arrow_forwardIn statistical thermodynamics, check the hcv following equality: ß Aɛ = KTarrow_forwardPlease correct answer and don't used hand raitingarrow_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 Learning
General, Organic, and Biological ChemistryChemistryISBN:9781285853918Author:H. Stephen StokerPublisher:Cengage Learning
Organic And Biological ChemistryChemistryISBN:9781305081079Author:STOKER, H. Stephen (howard Stephen)Publisher: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
General, Organic, and Biological Chemistry
Chemistry
ISBN:9781285853918
Author:H. Stephen Stoker
Publisher:Cengage Learning
Organic And Biological Chemistry
Chemistry
ISBN:9781305081079
Author:STOKER, H. Stephen (howard Stephen)
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
Nucleic acids - DNA and RNA structure; Author: MEDSimplified;https://www.youtube.com/watch?v=0lZRAShqft0;License: Standard YouTube License, CC-BY