Connect One Semester Access Card for General, Organic, & Biological Chemistry
4th Edition
ISBN: 9781260194654
Author: Janice Gorzynski Smith Dr.
Publisher: McGraw-Hill Education
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Question
Chapter 23, Problem 70P
Interpretation Introduction
Interpretation:
The reason for the citric acid cycle to be considered as a part of aerobic catabolic pathways needs to be explained.
Concept introduction:
The citric acid cycle is also known as the TCA or the Krebs contains numerous
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Students have asked these similar questions
1.
Answer the questions about the following reaction:
(a) Draw in the arrows that can be used make this reaction occur and draw in the product of substitution in this
reaction. Be sure to include any relevant stereochemistry in the product structure.
+
SK
F
Br
+
(b) In which solvent would this reaction proceed the fastest (Circle one)
Methanol
Acetone
(c) Imagine that you are working for a chemical company and it was your job to perform a similar reaction to the
one above, with the exception of the S atom in this reaction being replaced by an O atom. During the reaction, you
observe the formation of three separate molecules instead of the single molecule obtained above. What is the likeliest
other products that are formed? Draw them in the box provided.
3. For the reactions below, draw the arrows corresponding to the transformations and draw in the boxes the reactants
or products as indicated. Note: Part A should have arrows drawn going from the reactants to the middle structure
and the arrows on the middle structure that would yield the final structure. For part B, you will need to draw in
the reactant before being able to draw the arrows corresponding to product formation.
A.
B.
Rearrangement
ΘΗ
2. Draw the arrows required to make the following reactions occur. Please ensure your arrows point from exactly
where you want to exactly where you want. If it is unclear from where arrows start or where they end, only partial
credit will be given. Note: You may need to draw in lone pairs before drawing the arrows.
A.
B.
H-Br
人
C
Θ
CI
H
Cl
Θ
+
Br
O
Chapter 23 Solutions
Connect One Semester Access Card for General, Organic, & Biological Chemistry
Ch. 23.2 - Prob. 23.1PCh. 23.3 - Prob. 23.2PCh. 23.3 - The phosphorylation of glucose to glucose...Ch. 23.3 - Prob. 23.3PCh. 23.3 - Use the values for the hydrolysis of creatine...Ch. 23.4 - Prob. 23.2PPCh. 23.4 - Prob. 23.5PCh. 23.4 - Prob. 23.6PCh. 23.4 - Prob. 23.7PCh. 23.4 - Prob. 23.8P
Ch. 23.5 - Prob. 23.3PPCh. 23.5 - Prob. 23.9PCh. 23.5 - Prob. 23.10PCh. 23.5 - Prob. 23.11PCh. 23.6 - Prob. 23.12PCh. 23.6 - At several points in the electron transport chain,...Ch. 23.6 - In which region of the mitochondrion-the matrix or...Ch. 23 - Prob. 15PCh. 23 - Explain why mitochondria are called the...Ch. 23 - Prob. 17PCh. 23 - Prob. 18PCh. 23 - Prob. 19PCh. 23 - Prob. 20PCh. 23 - What are coupled reactions and why does coupling...Ch. 23 - Prob. 22PCh. 23 - Prob. 23PCh. 23 - Prob. 24PCh. 23 - Prob. 25PCh. 23 - Prob. 26PCh. 23 - Prob. 27PCh. 23 - Prob. 28PCh. 23 - Prob. 29PCh. 23 - Prob. 30PCh. 23 - Prob. 31PCh. 23 - Prob. 32PCh. 23 - (a) Draw the structure of the high-energy...Ch. 23 - Prob. 34PCh. 23 - Classify each substance as an oxidizing agent, a...Ch. 23 - Classify each substance as an oxidizing agent, a...Ch. 23 - When a substrate is oxidized, is NAD+ oxidized or...Ch. 23 - When a substrate is reduced, is FADH2 oxidized or...Ch. 23 - Prob. 39PCh. 23 - Prob. 40PCh. 23 - Prob. 41PCh. 23 - Prob. 42PCh. 23 - Prob. 43PCh. 23 - Prob. 44PCh. 23 - Prob. 45PCh. 23 - Prob. 46PCh. 23 - The conversion of isocitrate to ketoglutarate in...Ch. 23 - Prob. 48PCh. 23 - Prob. 49PCh. 23 - Prob. 50PCh. 23 - Prob. 51PCh. 23 - What is the role of each of the following in the...Ch. 23 - What is the role of each of the following in the...Ch. 23 - Prob. 54PCh. 23 - Prob. 55PCh. 23 - Prob. 56PCh. 23 - Prob. 57PCh. 23 - Prob. 58PCh. 23 - Prob. 59PCh. 23 - Prob. 60PCh. 23 - Prob. 61PCh. 23 - Prob. 62PCh. 23 - Prob. 63PCh. 23 - Prob. 64PCh. 23 - Prob. 65PCh. 23 - Prob. 66PCh. 23 - Prob. 67PCh. 23 - Prob. 68PCh. 23 - Prob. 69PCh. 23 - Prob. 70PCh. 23 - Prob. 71PCh. 23 - Prob. 72PCh. 23 - Prob. 73PCh. 23 - Prob. 74PCh. 23 - Prob. 75CPCh. 23 - Prob. 76CP
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- Answers to the remaining 6 questions will be hand-drawn on paper and submitted as a single file upload below: Review of this week's reaction: H₂NCN (cyanamide) + CH3NHCH2COOH (sarcosine) + NaCl, NH4OH, H₂O ---> H₂NC(=NH)N(CH3)CH2COOH (creatine) Q7. Draw by hand the reaction of creatine synthesis listed above using line structures without showing the Cs and some of the Hs, but include the lone pairs of electrons wherever they apply. (4 pts) Q8. Considering the Zwitterion form of an amino acid, draw the Zwitterion form of Creatine. (2 pts) Q9. Explain with drawing why the C-N bond shown in creatine structure below can or cannot rotate. (3 pts) NH2(C=NH)-N(CH)CH2COOH This bond Q10. Draw two tautomers of creatine using line structures. (Note: this question is valid because problem Q9 is valid). (4 pts) Q11. Mechanism. After seeing and understanding the mechanism of creatine synthesis, students should be ready to understand the first half of one of the Grignard reactions presented in a past…arrow_forwardPropose a synthesis pathway for the following transformations. b) c) d)arrow_forwardThe rate coefficient of the gas-phase reaction 2 NO2 + O3 → N2O5 + O2 is 2.0x104 mol–1 dm3 s–1 at 300 K. Indicate whether the order of the reaction is 0, 1, or 2.arrow_forward
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- In the drawing area below, draw the major products of this organic reaction: 1. NaOH ? 2. CH3Br If there are no major products, because nothing much will happen to the reactant under these reaction conditions, check the box under the drawing area instead. No reaction. Click and drag to start drawing a structure. ☐ : A คarrow_forwardPredict the major products of the following organic reaction: NC 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 draw bonds carefully to show important geometric relationships between substituents. Note: if your answer contains a complicated ring structure, you must use one of the molecular fragment stamps (available in the menu at right) to enter the ring structure. You can add any substituents using the pencil tool in the usual way. Click and drag to start drawing a structure. Х аarrow_forwardPredict the major products of this organic reaction. Be sure you use dash and wedge bonds to show stereochemistry where it's important. + ☑ OH 1. TsCl, py .... 文 P 2. t-BuO K Click and drag to start drawing a structure.arrow_forward
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