Student Solutions Manual for Oxtoby/Gillis/Butler's Principles of Modern Chemistry, 8th
Student Solutions Manual for Oxtoby/Gillis/Butler's Principles of Modern Chemistry, 8th
8th Edition
ISBN: 9798214170251
Author: David W. Oxtoby, H. Pat Gillis and Laurie J. Butler
Publisher: Cengage Learning US
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Chapter 7, Problem 40AP

Consider the following proposed structures for benzene, each of which is consistent with the molecular formula C 6 H 6 .

Chapter 7, Problem 40AP, Consider the following proposed structures for benzene, each of which is consistent with the

(iv) CH 3 C C C C CH 3

(v) CH 2 = CH C CH = CH 2

When benzene reacts with chlorine to give C 6 H 5 Cl,

  1. only one isomer of that compound forms. Which of the five proposed structures for benzene are consistent with this observation?
  2. When C 6 H 5 Cl reacts further with chlorine to give C 6 H 4 Cl 2 , exactly three isomers of the latter compound form. Which of the five proposed structures for benzene are consistent with this observation?

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need help please and thanks dont understand only need help with C-F Learning Goal: As discussed during the lecture, the enzyme HIV-1 reverse transcriptae (HIV-RT) plays a significant role for the HIV virus and is an important drug target. Assume a concentration [E] of 2.00 µM (i.e. 2.00 x 10-6 mol/l) for HIV-RT. Two potential drug molecules, D1 and D2, were identified, which form stable complexes with the HIV-RT. The dissociation constant of the complex ED1 formed by HIV-RT and the drug D1 is 1.00 nM (i.e. 1.00 x 10-9). The dissociation constant of the complex ED2 formed by HIV-RT and the drug D2 is 100 nM (i.e. 1.00 x 10-7).   Part A - Difference in binding free eenergies Compute the difference in binding free energy (at a physiological temperature T=310 K) for the complexes. Provide the difference as a positive numerical expression with three significant figures in kJ/mol. The margin of error is 2%.   Part B - Compare difference in free energy to the thermal…
Please correct answer and don't used hand raiting
need help please and thanks dont understand a-b Learning Goal: As discussed during the lecture, the enzyme HIV-1 reverse transcriptae (HIV-RT) plays a significant role for the HIV virus and is an important drug target. Assume a concentration [E] of 2.00 µM (i.e. 2.00 x 10-6 mol/l) for HIV-RT. Two potential drug molecules, D1 and D2, were identified, which form stable complexes with the HIV-RT. The dissociation constant of the complex ED1 formed by HIV-RT and the drug D1 is 1.00 nM (i.e. 1.00 x 10-9). The dissociation constant of the complex ED2 formed by HIV-RT and the drug D2 is 100 nM (i.e. 1.00 x 10-7).   Part A - Difference in binding free eenergies Compute the difference in binding free energy (at a physiological temperature T=310 K) for the complexes. Provide the difference as a positive numerical expression with three significant figures in kJ/mol. The margin of error is 2%.   Part B - Compare difference in free energy to the thermal energy Divide the…

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Student Solutions Manual for Oxtoby/Gillis/Butler's Principles of Modern Chemistry, 8th

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