Homework Answers
Add Answer to:
Q7) Below is the structure of an unknown mole me substituents Russure of an unknown molecule...
can you help me answer this question? Click the "draw structure" button to launch the drawing...
can
you help me answer this question?
Click the "draw structure" button to launch the drawing utility. Report problem Compound B has the molecular formula C,H, 0. Identify the structure from the H NMR and IR spectra given. TH NMR of 11 10 9 8 7 IR of B Transmittance 4000 3000 1000 3000 2500 2000 1500 Wavenumber(cm)
IR Worksheet 1. For each spectrum below: 1) Label the major peaks with their approximate frequency....
IR Worksheet 1. For each spectrum below: 1) Label the major peaks with their approximate frequency. 2) Identify the bond vibration and possible functional group associated with each peak. 3) Match the spectra to one of these possible compounds: NH2 TRANSMITTANCE[%] pobo edo "2060 bo zdoo 160 Tobo 560 WAVENUMBER [cm-1] oot 08 TRANSMITTANCE [%] 09 01 02 4000 3500 3000 2500 2000 WAVENUMBER (cm-1] 1500 1000 500 οοο TRANSMITTANCE (6) οο οο οε 4000 3500 3000 1500 1000 2500...
14.73 An unknown alcohol was treated with chromic acid to give a product with the following...
14.73 An unknown alcohol was treated with chromic acid to give a product with the following IR spectrum. Which of the following state- ments must be true? 100 % Transmittance 0 + 4000 3500 1500 1000 3000 2500 2000 Wavenumber (cm-") (a) The unknown compound must be a primary alcohol. (b) The unknown compound must be a secondary alcohol. (c) The unknown compound must be a tertiary alcohol. (d) The unknown compound must be acyclic.
Identify the peaks that identify the functional groups in the IR spectrum Unknown 4 C2H60 TRANSMITTANCE...
Identify the peaks that identify the functional groups
in the IR spectrum
Unknown 4 C2H60 TRANSMITTANCE 1001- 0 900- 0 800- 0.700- 0.600- 0.500- 0.400- 0.300- 0200- 0.100- 0.000- 4000 IR Unknown 3500 3000 2500 2000 1000 1500 Load IR spectrum Load proton NMR Show structure Spectra are displayed using JSpecView Website maintained by Jennifer Muzyka Contact me at jennifer muzyka@centre edu. Unknown 5 C3H5NO TRANSMITTANCE 1.001 - 0.900- 0800- 0.700- 0.600- 0.500- 0.400- 0.300- 0 200- 0.100- 0 000...
could you please help me to explain the problem with answers and explain why peak c...
could you please help me to explain the problem with
answers and explain why peak c is 3h triplets ?
points) A compound, C&H-N, has the following IR and 'H NMR spectra. 100 momw Transmittance %) 0 TTT 500 1000 4000 3500 3000 2500 2000 1500 Wavenumber (cm) peak a: 2H, triplet peak b: 2H, multiplet peak c: 3H, triplet Intensity - TMS (a) (8 points) Calculate the degree of unsaturation for this compound. Degree of unsaturation = 2 (b)...
Can you please figure out what the unknown compound is with relevant peaks in the given...
Can you please figure out what the unknown
compound is with relevant peaks in the given H-NMR, C-NMR, and IR
with given temperatures? Thank you in advance.
1H NMR 3 PPM 13C NMR 45 40 35 30 20 15 10 5 25 PPM El-MS: 73.1 MP = -50°C BP = 55.5°C SciFinder® .100 100 08 ....80 TRANSMITTANCE [%] 60 40 20 4000 2000- 3500 3500 3000 3000 1500 1000 500 2500 2000 WAVENUMBER [cm-1]
6. An unknown compound, CsH10O2, gives the NMR and IR shown below. Propose a structure. wavelength...
6. An unknown compound, CsH10O2, gives the NMR and IR shown below. Propose a structure. wavelength (m) 9 10 11 12 13 14 15 16 100 80 60 40 20 ol 4000 3500 3000 2500 1400 1200 1000 800 2000 1800 1600 wavenumber(cm) 600 SOHE 5.5.6 7.11 70 690 200 156 LA 1.6 10 8 (ppm)
Assign the peak for both of the IR spectrum below and identify what compound is this...
Assign the peak for both of the IR spectrum below and identify
what compound is this and draw the structure of the compound.
100 90 80 70 W 60 50 % Transmission 40 30 - 923 1677 1285 20 - 702 10 0 4000 3500 3000 2500 2000 1500 1000 Wavenumber (cm) 100 80 m % Transmission 1660 1209 1438 886 757 0 4000 3500 3000 2500 1500 1000 2000 Wavenumber (cm*')
perpose a structure with a formula of C5H12O with the given information % Transmittance 0 4000...
perpose a structure with a formula of C5H12O with the
given information
% Transmittance 0 4000 3500 3000 1500 1000 2500 2000 Wavenumber 1. Propose a structure for a compound with molecular formula C3H120 that exhibits the following 13C- NMR and IR spectra Carbon 13 NMR 73.8 100 90 80 70 60 50 40 Chemical shift (ppm) 30 20 10 0
Use the spectra below to determine the molecular formula and chemical structure of the unknown compound....
Use the spectra below to determine the molecular formula and
chemical structure of the unknown compound.
MASS 142 % of Base Peak 1147 40 50 70 80 5 100 % Transmittance Jari- 3000 1000 4000 'H NMR 300 MERE 2000 Wavenumber (cm) 3.0 25 20 15 Ppm 4.0 3.5 C/DEPT NMR 75.5 MHz ppm 60 50 40 80 70 90 100 110 120 170 160 150 140 130 ppm 4.5 4.0 3.5 3.0 2.5 2.0 1.5 ppm COSY 300 MHz...
can
you help me answer this question?
Click the "draw structure" button to launch the drawing utility. Report problem Compound B has the molecular formula C,H, 0. Identify the structure from the H NMR and IR spectra given. TH NMR of 11 10 9 8 7 IR of B Transmittance 4000 3000 1000 3000 2500 2000 1500 Wavenumber(cm)
IR Worksheet 1. For each spectrum below: 1) Label the major peaks with their approximate frequency. 2) Identify the bond vibration and possible functional group associated with each peak. 3) Match the spectra to one of these possible compounds: NH2 TRANSMITTANCE[%] pobo edo "2060 bo zdoo 160 Tobo 560 WAVENUMBER [cm-1] oot 08 TRANSMITTANCE [%] 09 01 02 4000 3500 3000 2500 2000 WAVENUMBER (cm-1] 1500 1000 500 οοο TRANSMITTANCE (6) οο οο οε 4000 3500 3000 1500 1000 2500...
14.73 An unknown alcohol was treated with chromic acid to give a product with the following IR spectrum. Which of the following state- ments must be true? 100 % Transmittance 0 + 4000 3500 1500 1000 3000 2500 2000 Wavenumber (cm-") (a) The unknown compound must be a primary alcohol. (b) The unknown compound must be a secondary alcohol. (c) The unknown compound must be a tertiary alcohol. (d) The unknown compound must be acyclic.
Identify the peaks that identify the functional groups
in the IR spectrum
Unknown 4 C2H60 TRANSMITTANCE 1001- 0 900- 0 800- 0.700- 0.600- 0.500- 0.400- 0.300- 0200- 0.100- 0.000- 4000 IR Unknown 3500 3000 2500 2000 1000 1500 Load IR spectrum Load proton NMR Show structure Spectra are displayed using JSpecView Website maintained by Jennifer Muzyka Contact me at jennifer muzyka@centre edu. Unknown 5 C3H5NO TRANSMITTANCE 1.001 - 0.900- 0800- 0.700- 0.600- 0.500- 0.400- 0.300- 0 200- 0.100- 0 000...
could you please help me to explain the problem with
answers and explain why peak c is 3h triplets ?
points) A compound, C&H-N, has the following IR and 'H NMR spectra. 100 momw Transmittance %) 0 TTT 500 1000 4000 3500 3000 2500 2000 1500 Wavenumber (cm) peak a: 2H, triplet peak b: 2H, multiplet peak c: 3H, triplet Intensity - TMS (a) (8 points) Calculate the degree of unsaturation for this compound. Degree of unsaturation = 2 (b)...
Can you please figure out what the unknown
compound is with relevant peaks in the given H-NMR, C-NMR, and IR
with given temperatures? Thank you in advance.
1H NMR 3 PPM 13C NMR 45 40 35 30 20 15 10 5 25 PPM El-MS: 73.1 MP = -50°C BP = 55.5°C SciFinder® .100 100 08 ....80 TRANSMITTANCE [%] 60 40 20 4000 2000- 3500 3500 3000 3000 1500 1000 500 2500 2000 WAVENUMBER [cm-1]
6. An unknown compound, CsH10O2, gives the NMR and IR shown below. Propose a structure. wavelength (m) 9 10 11 12 13 14 15 16 100 80 60 40 20 ol 4000 3500 3000 2500 1400 1200 1000 800 2000 1800 1600 wavenumber(cm) 600 SOHE 5.5.6 7.11 70 690 200 156 LA 1.6 10 8 (ppm)
Assign the peak for both of the IR spectrum below and identify
what compound is this and draw the structure of the compound.
100 90 80 70 W 60 50 % Transmission 40 30 - 923 1677 1285 20 - 702 10 0 4000 3500 3000 2500 2000 1500 1000 Wavenumber (cm) 100 80 m % Transmission 1660 1209 1438 886 757 0 4000 3500 3000 2500 1500 1000 2000 Wavenumber (cm*')
perpose a structure with a formula of C5H12O with the
given information
% Transmittance 0 4000 3500 3000 1500 1000 2500 2000 Wavenumber 1. Propose a structure for a compound with molecular formula C3H120 that exhibits the following 13C- NMR and IR spectra Carbon 13 NMR 73.8 100 90 80 70 60 50 40 Chemical shift (ppm) 30 20 10 0
Use the spectra below to determine the molecular formula and
chemical structure of the unknown compound.
MASS 142 % of Base Peak 1147 40 50 70 80 5 100 % Transmittance Jari- 3000 1000 4000 'H NMR 300 MERE 2000 Wavenumber (cm) 3.0 25 20 15 Ppm 4.0 3.5 C/DEPT NMR 75.5 MHz ppm 60 50 40 80 70 90 100 110 120 170 160 150 140 130 ppm 4.5 4.0 3.5 3.0 2.5 2.0 1.5 ppm COSY 300 MHz...
Most questions answered within 3 hours.
-
The chickens at Colonel Thompson's Ranch have a mean weight of
1850 g, with a standard...
asked 35 seconds ago -
22.3 g of fructose, C6H12O6,
are dissolved completely in 75.5 mL of pure water at 20.0...
asked 26 minutes ago -
There are many minerals which contain sliver. One of them,
smithite, is placed in water and...
asked 3 minutes ago -
Two bankrobbers are standing side by side, trying to push open
the door of a safe...
asked 27 minutes ago -
The time married men with children spend on child care averages
5.9 hours per week (Time,...
asked 5 minutes ago -
2. You want to buy a house. You can make an initial payment of
$200,000 and...
asked 24 minutes ago -
Why study the ‘Economic environment’ of a country? Describe the
information you will be collecting in...
asked 15 minutes ago -
A chandelier with mass m is suspended from a cable with mass M
from the ceiling....
asked 25 minutes ago -
How many disk accesses are needed to bring byte i of a file
into memory when...
asked 28 minutes ago -
Compare/Contrast the Lac and Ara operons.
asked 44 minutes ago -
Part A
What is the maximum speed with which a 1200-kg car can round a
turn...
asked 45 minutes ago -
Write in c++ please
Read and write 5 students information such as, Student
ID, first name,...
asked 44 minutes ago