Homework Answers
In mass spectrum we are not getting splitting pattern we getting ions ,in nmr splitting is take place because of adjacent hydrogen atoms.
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4-methylbenzaldehyde can someone explain all the splitting patterns
present in the mass spectrum, aka why...
Please match the compound to its spectrum and explain why cpd 22 Spectrum A 100- 60...
Please match the compound to its spectrum and explain
why
cpd 22 Spectrum A 100- 60 40 20 100 125 50 75 m/z Spectrum B 100 80- 60 40 20- 10 20 30 40 50 60 70 0 90 100 110 120 m/z (6 points) Match EOT Spectrum C 100- 80- 60 40 75 100 125 50 m/z Spectrum D 100 80 60- 40 20- 25 50 75 100 125 m/z Spectrum E 100 80 60 20 10 20 30...
Use the mass spectrum to answer the questions below Does the compound contain chlorine or bromine...
Use the mass spectrum to answer the questions below
Does the compound contain chlorine or bromine or neither?
Explain.
Give the m/z value for the molecular ion peak.
Give the m/z value for the base peak.
The base peak is a common fragment – what is the most likely
chemical formula for the base peak?
Does the compound contain chlorine or bromine or neither?
Explain.
Give the m/z value for the molecular ion peak.
Give the m/z value for the...
Question1) identify the name of the compound represented on the spectrum graph? Question2) For CNMR, indicate how many types of carbon atoms present and the identity of characteristics peaks? Quest...
Question1) identify the name of the compound represented on
the spectrum graph?
Question2) For CNMR, indicate how many types of carbon atoms
present and the identity of characteristics peaks?
Question3) For HNMR, indicate ho many types of carbon atoms
present, the different identity of characteristics peaks, and
explanations of it various splitting patterns?
Question4) Also for IR, indicate the identity of it
characteristics peaks
Question5) Finally for MS, Identify the parent peak, the
molecular weight and it implication, the most...
can someone explain this H NMR spectrum why does b not follow the n+1 rule is...
can someone explain this H NMR spectrum why does b not
follow the n+1 rule is it do to symmetry? can someone explain this
concept to me
• A urugens are located within an unresolved cluster of peaks the methyl peaks can e chemical shifts (higher field). However, even when methyl ognized as tall singlets, doublets, or triplets clearly emerging from the a types of protons. Methine protons are usually separated from the doublets, or triplets clearly emerging from the...
Unknown 315-S20-2 Can someone help me fill out the table on the right side please IR...
Unknown 315-S20-2
Can someone help me fill out the table on the right side
please
IR Spectrum:
Unknown # 315-S20-2 Mol. Wt. = 181.0 g/mol C-33.17% H=5.01% 0 = 17.68% Molecular Formula Degree of Unsaturation = Mass Spectrum IR spectrum (liquid film) 100- Relative Intensity 150 175 25 50 75 100 125 m/z Based on the M.W., circle & label the molecular ion peak (M). Spectrum Region Frequency (cm ) Peak Shape (sharp, broad) MAVUTO Peak Intensity (strong, med., weak)...
List all the clues that you can gather on the composition of the molecule whose spectrum...
List all the clues that you can gather on the composition of the
molecule whose spectrum is shown below:
List out all the clues that you can gather on the composition of the molecule whose spectrum is shown below: (4 pts) 105 100 MS-NW-9938 169 80 184 186 D 60 40 51 90 20- 122 100 175 25 50 75 125 150 m/z
Can someone explain to me why there is a peak pointed upwards on this IR spectrum...
Can someone explain to me why there is a peak pointed upwards on
this IR spectrum data sheet? Could it be because the salt plates
were scratched or thin?
%T 13 15 70 4000.6 3000 1000 649.893 2000 Wavenumber [cm-1]
Mass Spectrum (not shown): [M] = 220 (75%), 222 (100%), 224 (25%) m/z IR Spectrum (not...
Mass Spectrum (not shown): [M] = 220 (75%), 222 (100%), 224
(25%) m/z
IR Spectrum (not shown): 3060, 2985, 1600, 1495 cm-1 (all listed
are strong (s) unless otherwise indicated)
Please explain how you determine the organic compound for the
info given. Please check your compound with Chemdraw to verify your
answer before posting your answer (if you have Chemdraw).
Thanks!
NMR Spectrum (400 MHz, CDCI, 25 C) t (J 8Hz) PPM 1H1H 1H 3H C NMR Spectrum (with DEPT,...
Use the mass spectrum and either the NMR spectrum or the IR spectrum to deduce the...
Use the mass spectrum and either the NMR spectrum or the IR
spectrum to deduce the structure of the following compound
(c) C8HO3H NMR, 300 MHz, 6.1 ppm (singlet, 2H), 6.9 ppm (doublet, 1H), and 7.3 ppm (singlet, 1H), 7.4 ppm (doublet, 1H), 9.8 ppm (singlet, 1H); significant IR absorbances at 1687, 1602, 1449, 1264, 1038, 929, and 815 cm1. 100 149 (150) 80 60 40 121 63 20 65 91 0 15 20 25 30 35 40 45 50...
Please explain the answer in details. 2. [5 marks] Use the mass spectrum (EI-MS) and the...
Please explain the answer in details.
2. [5 marks] Use the mass spectrum (EI-MS) and the additional 'H NMR data to deduce the structure of the compound of the formula CgH603. 100 - 149 м (150) Relative Abundance (percent) 0+ரார்ராராராரா T ITIIIIIIIIIIIIIIIIINITITTITTTTTTTTTTTTTTTTTTTTTin 15 20 25 30 35 40 45 50 55 60 65 70 75 80 85 90 95 100 105 110 115 120 125 130 135 140 145 150 155 mz doublet singlet doublet
Please match the compound to its spectrum and explain
why
cpd 22 Spectrum A 100- 60 40 20 100 125 50 75 m/z Spectrum B 100 80- 60 40 20- 10 20 30 40 50 60 70 0 90 100 110 120 m/z (6 points) Match EOT Spectrum C 100- 80- 60 40 75 100 125 50 m/z Spectrum D 100 80 60- 40 20- 25 50 75 100 125 m/z Spectrum E 100 80 60 20 10 20 30...
Use the mass spectrum to answer the questions below
Does the compound contain chlorine or bromine or neither?
Explain.
Give the m/z value for the molecular ion peak.
Give the m/z value for the base peak.
The base peak is a common fragment – what is the most likely
chemical formula for the base peak?
Does the compound contain chlorine or bromine or neither?
Explain.
Give the m/z value for the molecular ion peak.
Give the m/z value for the...
Question1) identify the name of the compound represented on
the spectrum graph?
Question2) For CNMR, indicate how many types of carbon atoms
present and the identity of characteristics peaks?
Question3) For HNMR, indicate ho many types of carbon atoms
present, the different identity of characteristics peaks, and
explanations of it various splitting patterns?
Question4) Also for IR, indicate the identity of it
characteristics peaks
Question5) Finally for MS, Identify the parent peak, the
molecular weight and it implication, the most...
can someone explain this H NMR spectrum why does b not
follow the n+1 rule is it do to symmetry? can someone explain this
concept to me
• A urugens are located within an unresolved cluster of peaks the methyl peaks can e chemical shifts (higher field). However, even when methyl ognized as tall singlets, doublets, or triplets clearly emerging from the a types of protons. Methine protons are usually separated from the doublets, or triplets clearly emerging from the...
Unknown 315-S20-2
Can someone help me fill out the table on the right side
please
IR Spectrum:
Unknown # 315-S20-2 Mol. Wt. = 181.0 g/mol C-33.17% H=5.01% 0 = 17.68% Molecular Formula Degree of Unsaturation = Mass Spectrum IR spectrum (liquid film) 100- Relative Intensity 150 175 25 50 75 100 125 m/z Based on the M.W., circle & label the molecular ion peak (M). Spectrum Region Frequency (cm ) Peak Shape (sharp, broad) MAVUTO Peak Intensity (strong, med., weak)...
List all the clues that you can gather on the composition of the
molecule whose spectrum is shown below:
List out all the clues that you can gather on the composition of the molecule whose spectrum is shown below: (4 pts) 105 100 MS-NW-9938 169 80 184 186 D 60 40 51 90 20- 122 100 175 25 50 75 125 150 m/z
Can someone explain to me why there is a peak pointed upwards on
this IR spectrum data sheet? Could it be because the salt plates
were scratched or thin?
%T 13 15 70 4000.6 3000 1000 649.893 2000 Wavenumber [cm-1]
Mass Spectrum (not shown): [M] = 220 (75%), 222 (100%), 224
(25%) m/z
IR Spectrum (not shown): 3060, 2985, 1600, 1495 cm-1 (all listed
are strong (s) unless otherwise indicated)
Please explain how you determine the organic compound for the
info given. Please check your compound with Chemdraw to verify your
answer before posting your answer (if you have Chemdraw).
Thanks!
NMR Spectrum (400 MHz, CDCI, 25 C) t (J 8Hz) PPM 1H1H 1H 3H C NMR Spectrum (with DEPT,...
Use the mass spectrum and either the NMR spectrum or the IR
spectrum to deduce the structure of the following compound
(c) C8HO3H NMR, 300 MHz, 6.1 ppm (singlet, 2H), 6.9 ppm (doublet, 1H), and 7.3 ppm (singlet, 1H), 7.4 ppm (doublet, 1H), 9.8 ppm (singlet, 1H); significant IR absorbances at 1687, 1602, 1449, 1264, 1038, 929, and 815 cm1. 100 149 (150) 80 60 40 121 63 20 65 91 0 15 20 25 30 35 40 45 50...
Please explain the answer in details.
2. [5 marks] Use the mass spectrum (EI-MS) and the additional 'H NMR data to deduce the structure of the compound of the formula CgH603. 100 - 149 м (150) Relative Abundance (percent) 0+ரார்ராராராரா T ITIIIIIIIIIIIIIIIIINITITTITTTTTTTTTTTTTTTTTTTTTin 15 20 25 30 35 40 45 50 55 60 65 70 75 80 85 90 95 100 105 110 115 120 125 130 135 140 145 150 155 mz doublet singlet doublet
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