Introduction to General, Organic and Biochemistry
12th Edition
ISBN: 9780357391594
Author: Frederick A. Bettelheim; William H. Brown; Mary K. Campbell
Publisher: Cengage Learning US
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Chapter 27, Problem 41P
Interpretation Introduction
Interpretation : The cause of cramps in muscles during fatigue should be determined.
Concept Introduction : Glycolysis is the first step that forms pyruvate. In the presence of oxygen means aerobic respiration, this pyruvate enters in the Krebs cycle and extracts energy in the form of electrons transfer.
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starting
material
target
If so, draw a synthesis below. If no synthesis using reagents ALEKS recognizes is possible, check the box under the drawing area.
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Explanation
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Relative Intensity
Part VI. consider the multi-step reaction below for compounds
A, B, and C.
These compounds were subjected to mass spectrometric analysis and
the following spectra for A, B, and C was obtained.
Draw the structure of B and C and match all three compounds
to the correct spectra.
Relative Intensity
Relative Intensity
100
HS-NJ-0547
80
60
31
20
S1
84
M+
absent
10
30
40
50
60
70
80
90
100
100-
MS2016-05353CM
80-
60
40
20
135 137
S2
164 166
0-m
25
50
75
100
125
150
m/z
60
100
MS-NJ-09-43
40
20
20
80
45
S3
25
50
75
100
125
150
175
m/z
Chapter 27 Solutions
Introduction to General, Organic and Biochemistry
Ch. 27.1 - Prob. 27.1QCCh. 27.2 - Prob. 27.2QCCh. 27.3 - Prob. 27.3QCCh. 27.4 - Prob. 27.4QCCh. 27.5 - Prob. 27.5QCCh. 27.6 - Prob. 27.6QCCh. 27.7 - Prob. 27.7QCCh. 27.8 - Prob. 27.8QCCh. 27.9 - Prob. 27.9QCCh. 27 - Prob. 1P
Ch. 27 - What are the products of lipase-catalyzed...Ch. 27 - What is the main use of amino acids in the body?Ch. 27 - Prob. 4PCh. 27 - Prob. 5PCh. 27 - Prob. 6PCh. 27 - Prob. 7PCh. 27 - Prob. 8PCh. 27 - Prob. 9PCh. 27 - Prob. 10PCh. 27 - Prob. 11PCh. 27 - Prob. 12PCh. 27 - Prob. 13PCh. 27 - Prob. 14PCh. 27 - Prob. 15PCh. 27 - Prob. 16PCh. 27 - Prob. 17PCh. 27 - Prob. 18PCh. 27 - Prob. 19PCh. 27 - Prob. 20PCh. 27 - Two enzymes participating in ß-oxidation have the...Ch. 27 - Prob. 22PCh. 27 - Prob. 23PCh. 27 - Is the ß -oxidation of fatty acid (without the...Ch. 27 - Calculate the number of ATP molecules obtained in...Ch. 27 - Prob. 26PCh. 27 - Prob. 27PCh. 27 - Prob. 28PCh. 27 - Prob. 29PCh. 27 - Prob. 30PCh. 27 - Prob. 31PCh. 27 - Prob. 32PCh. 27 - Prob. 33PCh. 27 - Ammonia, NH3, and ammonium ion, NH+4are both...Ch. 27 - Prob. 35PCh. 27 - Prob. 36PCh. 27 - Prob. 37PCh. 27 - Prob. 38PCh. 27 - 28-39 The metabolism of the carbon skeleton of...Ch. 27 - Prob. 40PCh. 27 - Prob. 41PCh. 27 - Prob. 42PCh. 27 - (Chemical Connections 27B ) Does gastric bypass...Ch. 27 - Prob. 44PCh. 27 - Prob. 45PCh. 27 - Prob. 46PCh. 27 - Prob. 47PCh. 27 - Prob. 48PCh. 27 - Prob. 49PCh. 27 - Prob. 50PCh. 27 - Prob. 51PCh. 27 - Prob. 52PCh. 27 - Prob. 53PCh. 27 - Write the products of the transamination reaction...Ch. 27 - Prob. 55PCh. 27 - Prob. 56PCh. 27 - Prob. 57PCh. 27 - Prob. 58PCh. 27 - Prob. 59PCh. 27 - Prob. 60PCh. 27 - Prob. 61PCh. 27 - Prob. 62PCh. 27 - Prob. 63PCh. 27 - Prob. 64PCh. 27 - Prob. 65PCh. 27 - Prob. 66PCh. 27 - Prob. 67PCh. 27 - Prob. 68PCh. 27 - Prob. 69PCh. 27 - Prob. 70PCh. 27 - Prob. 71PCh. 27 - Prob. 72PCh. 27 - Prob. 73PCh. 27 - Prob. 74PCh. 27 - Prob. 75PCh. 27 - Many soft drinks contain citric acid to add...Ch. 27 - Prob. 77PCh. 27 - Prob. 78PCh. 27 - Prob. 79PCh. 27 - Prob. 80P
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- Part II. Given two isomers: 2-methylpentane (A) and 2,2-dimethyl butane (B) answer the following: (a) match structures of isomers given their mass spectra below (spectra A and spectra B) (b) Draw the fragments given the following prominent peaks from each spectrum: Spectra A m/2 =43 and 1/2-57 spectra B m/2 = 43 (c) why is 1/2=57 peak in spectrum A more intense compared to the same peak in spectrum B. Relative abundance Relative abundance 100 A 50 29 29 0 10 -0 -0 100 B 50 720 30 41 43 57 71 4-0 40 50 60 70 m/z 43 57 8-0 m/z = 86 M 90 100 71 m/z = 86 M -O 0 10 20 30 40 50 60 70 80 -88 m/z 90 100arrow_forwardPart IV. C6H5 CH2CH2OH is an aromatic compound which was subjected to Electron Ionization - mass spectrometry (El-MS) analysis. Prominent m/2 values: m/2 = 104 and m/2 = 9) was obtained. Draw the structures of these fragments.arrow_forwardFor each reaction shown below follow the curved arrows to complete each equationby showing the structure of the products. Identify the acid, the base, the conjugated acid andconjugated base. Consutl the pKa table and choose the direciton theequilibrium goes. However show the curved arrows. Please explain if possible.arrow_forward
- A molecule shows peaks at 1379, 1327, 1249, 739 cm-1. Draw a diagram of the energy levels for such a molecule. Draw arrows for the possible transitions that could occur for the molecule. In the diagram imagine exciting an electron, what are its various options for getting back to the ground state? What process would promote radiation less decay? What do you expect for the lifetime of an electron in the T1 state? Why is phosphorescence emission weak in most substances? What could you do to a sample to enhance the likelihood that phosphorescence would occur over radiationless decay?arrow_forwardRank the indicated C—C bonds in increasing order of bond length. Explain as why to the difference.arrow_forwardUse IUPAC rules to name the following alkanearrow_forward
- Please correct answer and don't use hand ratingarrow_forwardPlease correct answer and don't use hand ratingarrow_forwardThe SN 1 mechanism starts with the rate-determining step which is the dissociation of the alkyl halide into a carbocation and a halide ion. The next step is the rapid reaction of the carbocation intermediate with the nucleophile; this step completes the nucleophilic substitution stage. The step that follows the nucleophilic substitution is a fast acid-base reaction. The nucleophile now acts as a base to remove the proton from the oxonium ion from the previous step, to give the observed product. Draw a curved arrow mechanism for the reaction, adding steps as necessary. Be sure to include all nonzero formal charges. Cl: Add/Remove step G Click and drag to start drawing a structure.arrow_forward
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