Draw the structure of the compound C,HgS from its proton ('H) NMR spectrum below. First-order spin-spin splitting rules and equal coupling constants can be assumed. (Detailed analysis of any non-first order portions of the spectrum will not be required.) Integral ratios to the nearest whole number are (left to right) 2:3:3. Used with permission from Aldrich Chemical Co., Inc. Solvent CDCI 9.0 7.5 6.0 1.5 0.0 Chemical shift, 8 (ppm) lle 610 1.273 2.515 2.103 You do not have to consider stereochemistry. You do not have to explicitly draw H atoms. Do not include lone pairs in your answer. They will not be considered in the grading. .. CH ChemDoodle Submit Answer Retry Entire Group 9 more group attempts remaining

Chemistry
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Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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Chapter1: Chemical Foundations
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Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Draw the structure of the compound C,HgS from its proton ('H) NMR spectrum below.
First-order spin-spin splitting rules and equal coupling constants can be assumed. (Detailed analysis of any non-first order portions of the spectrum will not be required.)
Integral ratios to the nearest whole number are (left to right) 2:3:3.
Used with permission from Aldrich Chemical Co., Inc.
Solvent CDCI
9.0
7.5
6.0
45
1.5
0.0
Chemical shift, 8 (ppm)
lle
610
1.273
2.515
2.103
You do not have to consider stereochemistry.
You do not have to explicitly draw H atoms.
Do not include lone pairs in your answer. They will not be considered in the grading.
..
CH4
ChemDoodle
Submit Answer
Retry Entire Group
9 more group attempts remaining
Transcribed Image Text:Draw the structure of the compound C,HgS from its proton ('H) NMR spectrum below. First-order spin-spin splitting rules and equal coupling constants can be assumed. (Detailed analysis of any non-first order portions of the spectrum will not be required.) Integral ratios to the nearest whole number are (left to right) 2:3:3. Used with permission from Aldrich Chemical Co., Inc. Solvent CDCI 9.0 7.5 6.0 45 1.5 0.0 Chemical shift, 8 (ppm) lle 610 1.273 2.515 2.103 You do not have to consider stereochemistry. You do not have to explicitly draw H atoms. Do not include lone pairs in your answer. They will not be considered in the grading. .. CH4 ChemDoodle Submit Answer Retry Entire Group 9 more group attempts remaining
Draw the structure of the compound C,H,0, from its proton ('H) NMR spectrum below.
First-order spin-spin splitting rules and equal coupling constants can be assumed. (Detailed analysis of any non-first order portions of the spectrum will not be required.)
Integral ratios to the nearest whole number are (left to right) 1:2:2:3.
Used with permission from Aldrich Chemical Co., Inc.
Solvent CDCIa
6.3
Chemical sbi, o (ppm)
12.5
10.4
8.3
4.2
2.1
0.0
2547
1.906
1.697
1.488
1.139
0.952
0.765
2.310
You do not have to consider stereochemistry.
You do not have to explicitly draw H atoms.
Do not include lone pairs in your answer. They will not be considered in the grading.
P
opy
aste
CH.
ChemDoodle
Submit Answer
Retry Entire Group
9 more group attempts remaining
Transcribed Image Text:Draw the structure of the compound C,H,0, from its proton ('H) NMR spectrum below. First-order spin-spin splitting rules and equal coupling constants can be assumed. (Detailed analysis of any non-first order portions of the spectrum will not be required.) Integral ratios to the nearest whole number are (left to right) 1:2:2:3. Used with permission from Aldrich Chemical Co., Inc. Solvent CDCIa 6.3 Chemical sbi, o (ppm) 12.5 10.4 8.3 4.2 2.1 0.0 2547 1.906 1.697 1.488 1.139 0.952 0.765 2.310 You do not have to consider stereochemistry. You do not have to explicitly draw H atoms. Do not include lone pairs in your answer. They will not be considered in the grading. P opy aste CH. ChemDoodle Submit Answer Retry Entire Group 9 more group attempts remaining
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