Bundle: Chemistry for Today: General, Organic, and Biochemistry, Loose-Leaf Version, 9th + LMS Integrated OWLv2, 4 terms (24 months) Printed Access Card
9th Edition
ISBN: 9781337598255
Author: Spencer L. Seager
Publisher: Cengage Learning
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Chapter 12, Problem 12.70E
Interpretation Introduction
Interpretation:
The generalized energy diagram for reaction of
Concept Introduction:
Endothermic reaction is a type of
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Learning Goal:
This question reviews the format for writing an element's written symbol. Recall that written symbols have a particular format. Written symbols use a form like this:
35 Cl
17
In this form the mass number, 35, is a stacked superscript. The atomic number, 17, is a stacked subscript. "CI" is the chemical symbol for the element chlorine. A general way to show this form is:
It is also correct to write symbols by leaving off the atomic number, as in the following form:
atomic number
mass number Symbol
35 Cl or
mass number Symbol
This is because if you write the element symbol, such as Cl, you know the atomic number is 17 from that symbol. Remember that the atomic number, or number of protons in the nucleus, is what defines the element. Thus, if 17 protons
are in the nucleus, the element can only be chlorine. Sometimes you will only see 35 C1, where the atomic number is not written.
Watch this video to review the format for written symbols.
In the following table each column…
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…
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…
Chapter 12 Solutions
Bundle: Chemistry for Today: General, Organic, and Biochemistry, Loose-Leaf Version, 9th + LMS Integrated OWLv2, 4 terms (24 months) Printed Access Card
Ch. 12 - Prob. 12.1ECh. 12 - Define the terms alkene, alkyne, and aromatic...Ch. 12 - Select those compounds that can be correctly...Ch. 12 - Prob. 12.4ECh. 12 - Give the IUPAC name for the following compounds:...Ch. 12 - Prob. 12.6ECh. 12 - Prob. 12.7ECh. 12 - Prob. 12.8ECh. 12 - Prob. 12.9ECh. 12 - Prob. 12.10E
Ch. 12 - Prob. 12.11ECh. 12 - Prob. 12.12ECh. 12 - What type of hybridized orbital is present on...Ch. 12 - What type of orbital overlaps to form a pi bond in...Ch. 12 - Prob. 12.15ECh. 12 - Explain the difference between geometric and...Ch. 12 - Draw structural formulas and give IUPAC names for...Ch. 12 - Prob. 12.18ECh. 12 - Which of the following alkenes can exist as...Ch. 12 - Draw structural formulas for the following:...Ch. 12 - Prob. 12.21ECh. 12 - In what ways are the physical properties of...Ch. 12 - Prob. 12.23ECh. 12 - Prob. 12.24ECh. 12 - Complete the following reactions. Where more than...Ch. 12 - Prob. 12.26ECh. 12 - Prob. 12.27ECh. 12 - What reagents would you use to prepare each of the...Ch. 12 - What is an important commercial application of...Ch. 12 - Prob. 12.30ECh. 12 - Terpin hydrate is used medicinally as an...Ch. 12 - Prob. 12.32ECh. 12 - Prob. 12.33ECh. 12 - Prob. 12.34ECh. 12 - Prob. 12.35ECh. 12 - Much of todays plumbing in newly built homes is...Ch. 12 - Prob. 12.37ECh. 12 - What type of hybridized orbital is present on...Ch. 12 - How many sigma bonds and how many pi bonds make up...Ch. 12 - Prob. 12.40ECh. 12 - Explain why geometric isomerism is not possible in...Ch. 12 - Give the common name and major uses of the...Ch. 12 - Describe the physical and chemical properties of...Ch. 12 - Prob. 12.44ECh. 12 - Prob. 12.45ECh. 12 - Prob. 12.46ECh. 12 - Prob. 12.47ECh. 12 - Prob. 12.48ECh. 12 - Limonene, which is present in citrus peelings, has...Ch. 12 - A disubstituted cycloalkane such as a exhibits...Ch. 12 - Prob. 12.51ECh. 12 - Prob. 12.52ECh. 12 - Give an IUPAC name for the following as...Ch. 12 - Give an IUPAC name for the following as...Ch. 12 - Name the following compounds, using the prefixed...Ch. 12 - Name the following compounds, using the prefixed...Ch. 12 - Name the following by numbering the benzene ring....Ch. 12 - Name the following by numbering the benzene ring....Ch. 12 - Prob. 12.59ECh. 12 - Write structural formulas for the following:...Ch. 12 - Prob. 12.61ECh. 12 - Prob. 12.62ECh. 12 - Prob. 12.63ECh. 12 - Prob. 12.64ECh. 12 - Prob. 12.65ECh. 12 - Prob. 12.66ECh. 12 - Prob. 12.67ECh. 12 - Prob. 12.68ECh. 12 - Prob. 12.69ECh. 12 - Prob. 12.70ECh. 12 - Prob. 12.71ECh. 12 - Prob. 12.72ECh. 12 - Prob. 12.73ECh. 12 - Prob. 12.74ECh. 12 - Prob. 12.75ECh. 12 - Prob. 12.76ECh. 12 - Prob. 12.77ECh. 12 - Prob. 12.78ECh. 12 - Prob. 12.79ECh. 12 - Prob. 12.80ECh. 12 - Prob. 12.81ECh. 12 - Prob. 12.82ECh. 12 - Prob. 12.83ECh. 12 - The compound CH2=CHCH2CH2CH3 is an example of: a....Ch. 12 - The correct structural for ethyne is: a. HC=CH b....Ch. 12 - Prob. 12.86E
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- Please correct answer and don't used hand raitingarrow_forwardneed 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…arrow_forwardPlease correct answer and don't used hand raitingarrow_forward
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