Please include the following information allow with the molecular structure of the unknown compound:
1. IR-Include the major peaks and indicate the stretch wavenumber and what bond it is.
2. UV-VIs- If there is a lambda max given, please briefly
indicate what structural element is contributing to it.
3. HNMR-Include proton label, chemical shift, multiplicity, and
integration.
4. CNMR- include the carbon label and the chemical shift.
Some additional information about the unknown compound:
Iodoform Test: Clear solution
Chromic Acid Test: Green ppt
Tollens Test: Silver deposits
Sodium Hydroxide Test: No change
Homework Answers
![(5) I Humr data 2.0 (s, 3H) 3 8.5(s, 1H) 3 6.3(, 1H) 3 = fcly] c=CFH c=c-ção 10:(dilH) 7 =c-c=0 aldehy ele Protes vicinally c](http://img.homeworklib.com/questions/a1d6a830-942b-11eb-bdf7-35feb14061ca.png?x-oss-process=image/resize,w_560)
Add Answer to:
Please include the following information allow with the
molecular structure of the unknown compound:
1. IR-Include...
Based on the following spectroscopic data of an unknown compound with molecular formula C8H6S, (i) determine...
Based on the following
spectroscopic data of an unknown compound with molecular formula
C8H6S, (i) determine the chemical structure of this compound; (ii)
assign all the signals in the 1H-NMR spectrum & 13C-NMR
spectrum. NMR is complete
۳۳-۳-rr-T-------- IR Spectrum (KBr disc) 4000 3000 1200 800 2000 1600 V (cm) M ** = 13 Mass Spectrum بالليليللليلعليا % of base peak CgHES 40 80 200 240 280 120 m 160 /e 13C NMR Spectrum (100.0 MHz, CDCI, solution) expansion DEPT...
Amswer all parts please QUICKLY 6. Use the spectral data given to identify the structure of the unknown compound wit...
Amswer all parts please QUICKLY
6. Use the spectral data given to identify the structure of the unknown compound with chemical formula (C12H1602). (20 points) TOODE UV Spectum: 2 = 240 nm MW = 192 g/mol, ( Ombre HH2DSIMH IR resonance: 1610, 1729 cm', 13C NMR Spectrum (1000 MHz, CDCI, solution) DEPT CH CH CH proton decoupled solvent 200 160 120 B0 40 08 (ppm) TH NMR Spectrum (400 MHZ COCI, solution) expansion 9 8.0 7.5 PPM 10 9 8...
Label the spectra and propose a structure for the compound. Compound 6 1 1755 IR Spectrum...
Label the spectra and propose a structure for the compound.
Compound 6 1 1755 IR Spectrum quid fim 1120 4000 3000 2000 V (cm 16001200800 ) Mass Spectrum So base peak M" 158 (<1%) No significant UV absorption above 220 nm C₂ H₂ 403 280 40 80 120 160 200 240 13C NMR Spectrum 150.0 MHz, CDCI, solution) DEPT Chut Chitch! proton decoupled 200 160 120 80 40 0 8 (ppm) TH NMR Spectrum 2200 MHZ. CDC, solution) 150 10...
Name: 6. Use the spectral data given to identify the structure of the unknown compound with...
Name: 6. Use the spectral data given to identify the structure of the unknown compound with chemical formula (C12H1602). (20 points) UV Spectum: 2 = 240 nm MW = 192 g/mol, IR resonance: 1610, 1729 cm, 13C NMR Spectrum (1000 MHZ COCI, solution DEPT CHA CHA CH prolon de coupled 200 160 120 08 (ppm) TH NMR Spectrum (400 M2. CDCI, tion) person folhas Ab 2 BC 75 PPM ܢܐ & TMS 109 7 5 8 (ppm)
Label the spectra and propose a structure for the compound. Compound 1 IR Spectrum liquid mi...
Label the spectra and propose a structure for the compound.
Compound 1 IR Spectrum liquid mi 4000 3000 2000 1600 1200 1200 V on Mass Spectrum UV Spectrum 2. max 252 mm (10910622) 2. max 257 nm (log, 2.3) 2 mar 262 nm (10910€ 2.2) 2. max 254 nm (1090€ 2.2) 2.mex 268 nm logo 2.0) solvent thanol M 150 Coto2 40 80 240 120 m 200 280 160 /e 13C NMR Spectrum (100 M-2. CDC, solution ansion DEPT CH...
Deduce the following structure of the compound given their IR, H1 NMR, 13C NMR spectra, and...
Deduce the following structure of the compound given their IR, H1
NMR, 13C NMR spectra, and assign IR functional group absorptions
and assign the structure's protons and carbons to their respective
spectral resonances.
Compound 4 Da- U6)+20 IR Spectrum Oquid fim) 1760 800 1200 2000 1600 3000 4000 v (cm) Mass Spectrum 100 43 No significant UV absorption above 220 nm M146 (1% ) 87 20 CH1004 280 40 80 120 m/e 160 200 240 13C NMR Spectrum (1000 MHz,...
Label the spectra and propose a structure for the compound. Compound 3 IR Spectrum quid 4000...
Label the spectra and propose a structure for the compound.
Compound 3 IR Spectrum quid 4000 3000 2000 V (cm 1000 ) 1200 800 of base peak more Cg H100 280 40 80 120 160 200 240 C NMR Spectrum 50. 0 00, DEPT Chi sont on GGL 200 160120 120 80 40 0 5 (ppm) TH NMR Spectrum (200 M . CDCI, solution 10 9 8 7 6 5 4 3 2 i 8 (ppm)
Find the compounds using NMR and IR: Problem 85 IR Spectrum (liquid fiim) 1720 1600 2000...
Find the compounds using NMR and IR:
Problem 85 IR Spectrum (liquid fiim) 1720 1600 2000 v (cm) 800 3000 1200 4000 100 Mass Spectrum 73 140 138 80 No significant UV 60 115 absorption above 220 nm 40 M 194/196 (1% ) 20 CeH1102Br 120 160 200 240 280 40 80 m/e 13C NMR Spectrum (50.0 MHz, CDCI, solution) DEPT CH, Cн, сн! solvent proton decoupled 8 (ppm) 160 120 40 200 80 H NMR Spectrum (200 MHz, CDCI,...
Label spectra and propose a structure for the compound. Compound 1 IR Spectrum liquid mi 4000 3000 2000 1600 1200 12...
Label spectra and propose a structure for the compound.
Compound 1 IR Spectrum liquid mi 4000 3000 2000 1600 1200 1200 V on Mass Spectrum UV Spectrum 2. max 252 mm (10910622) 2. max 257 nm (log, 2.3) 2 mar 262 nm (10910€ 2.2) 2. max 254 nm (1090€ 2.2) 2.mex 268 nm logo 2.0) solvent thanol M 150 Coto2 40 80 240 120 m 200 280 160 /e 13C NMR Spectrum (100 M-2. CDC, solution ansion DEPT CH chut...
) A compound with molecular formula CxH 1403 displays the following spectral data. Propose a structure...
) A compound with molecular formula CxH 1403 displays the following spectral data. Propose a structure for this compound in the box at the bottom of the page. Peak assignments written on the spectra may be worth partial credit. (5 marks) r IR Spectrum liquid film) 1735 1717 4000 3000 1200 800 2000 1600 V (cm) 13C NMR Spectrum (100 MHz, CDCI, solution) DEPT CHI Chit Cht solvent proton decoupled 100 no Sloml proton decoupled 200 160 120 80 40...
Based on the following
spectroscopic data of an unknown compound with molecular formula
C8H6S, (i) determine the chemical structure of this compound; (ii)
assign all the signals in the 1H-NMR spectrum & 13C-NMR
spectrum. NMR is complete
۳۳-۳-rr-T-------- IR Spectrum (KBr disc) 4000 3000 1200 800 2000 1600 V (cm) M ** = 13 Mass Spectrum بالليليللليلعليا % of base peak CgHES 40 80 200 240 280 120 m 160 /e 13C NMR Spectrum (100.0 MHz, CDCI, solution) expansion DEPT...
Amswer all parts please QUICKLY
6. Use the spectral data given to identify the structure of the unknown compound with chemical formula (C12H1602). (20 points) TOODE UV Spectum: 2 = 240 nm MW = 192 g/mol, ( Ombre HH2DSIMH IR resonance: 1610, 1729 cm', 13C NMR Spectrum (1000 MHz, CDCI, solution) DEPT CH CH CH proton decoupled solvent 200 160 120 B0 40 08 (ppm) TH NMR Spectrum (400 MHZ COCI, solution) expansion 9 8.0 7.5 PPM 10 9 8...
Label the spectra and propose a structure for the compound.
Compound 6 1 1755 IR Spectrum quid fim 1120 4000 3000 2000 V (cm 16001200800 ) Mass Spectrum So base peak M" 158 (<1%) No significant UV absorption above 220 nm C₂ H₂ 403 280 40 80 120 160 200 240 13C NMR Spectrum 150.0 MHz, CDCI, solution) DEPT Chut Chitch! proton decoupled 200 160 120 80 40 0 8 (ppm) TH NMR Spectrum 2200 MHZ. CDC, solution) 150 10...
Name: 6. Use the spectral data given to identify the structure of the unknown compound with chemical formula (C12H1602). (20 points) UV Spectum: 2 = 240 nm MW = 192 g/mol, IR resonance: 1610, 1729 cm, 13C NMR Spectrum (1000 MHZ COCI, solution DEPT CHA CHA CH prolon de coupled 200 160 120 08 (ppm) TH NMR Spectrum (400 M2. CDCI, tion) person folhas Ab 2 BC 75 PPM ܢܐ & TMS 109 7 5 8 (ppm)
Label the spectra and propose a structure for the compound.
Compound 1 IR Spectrum liquid mi 4000 3000 2000 1600 1200 1200 V on Mass Spectrum UV Spectrum 2. max 252 mm (10910622) 2. max 257 nm (log, 2.3) 2 mar 262 nm (10910€ 2.2) 2. max 254 nm (1090€ 2.2) 2.mex 268 nm logo 2.0) solvent thanol M 150 Coto2 40 80 240 120 m 200 280 160 /e 13C NMR Spectrum (100 M-2. CDC, solution ansion DEPT CH...
Deduce the following structure of the compound given their IR, H1
NMR, 13C NMR spectra, and assign IR functional group absorptions
and assign the structure's protons and carbons to their respective
spectral resonances.
Compound 4 Da- U6)+20 IR Spectrum Oquid fim) 1760 800 1200 2000 1600 3000 4000 v (cm) Mass Spectrum 100 43 No significant UV absorption above 220 nm M146 (1% ) 87 20 CH1004 280 40 80 120 m/e 160 200 240 13C NMR Spectrum (1000 MHz,...
Label the spectra and propose a structure for the compound.
Compound 3 IR Spectrum quid 4000 3000 2000 V (cm 1000 ) 1200 800 of base peak more Cg H100 280 40 80 120 160 200 240 C NMR Spectrum 50. 0 00, DEPT Chi sont on GGL 200 160120 120 80 40 0 5 (ppm) TH NMR Spectrum (200 M . CDCI, solution 10 9 8 7 6 5 4 3 2 i 8 (ppm)
Find the compounds using NMR and IR:
Problem 85 IR Spectrum (liquid fiim) 1720 1600 2000 v (cm) 800 3000 1200 4000 100 Mass Spectrum 73 140 138 80 No significant UV 60 115 absorption above 220 nm 40 M 194/196 (1% ) 20 CeH1102Br 120 160 200 240 280 40 80 m/e 13C NMR Spectrum (50.0 MHz, CDCI, solution) DEPT CH, Cн, сн! solvent proton decoupled 8 (ppm) 160 120 40 200 80 H NMR Spectrum (200 MHz, CDCI,...
Label spectra and propose a structure for the compound.
Compound 1 IR Spectrum liquid mi 4000 3000 2000 1600 1200 1200 V on Mass Spectrum UV Spectrum 2. max 252 mm (10910622) 2. max 257 nm (log, 2.3) 2 mar 262 nm (10910€ 2.2) 2. max 254 nm (1090€ 2.2) 2.mex 268 nm logo 2.0) solvent thanol M 150 Coto2 40 80 240 120 m 200 280 160 /e 13C NMR Spectrum (100 M-2. CDC, solution ansion DEPT CH chut...
) A compound with molecular formula CxH 1403 displays the following spectral data. Propose a structure for this compound in the box at the bottom of the page. Peak assignments written on the spectra may be worth partial credit. (5 marks) r IR Spectrum liquid film) 1735 1717 4000 3000 1200 800 2000 1600 V (cm) 13C NMR Spectrum (100 MHz, CDCI, solution) DEPT CHI Chit Cht solvent proton decoupled 100 no Sloml proton decoupled 200 160 120 80 40...
Most questions answered within 3 hours.
-
Given a standardized normal distribution (with μ = 0 and a σ =
1), what is...
asked 24 minutes ago -
Given the following information:
acetic acid
CH3COOH
Ka = 1.8×10-5
triethylamine
(C2H5)3N
Kb = 5.2×10-4
(1)...
asked 10 minutes ago -
Potassium permanganate(KMNO4)is has a solubility of 6.4 g/ 100 g
of water at 20ºC, and 250...
asked 7 minutes ago -
51.
As the marginal propensity to expend rises, the multiplier:
decreases.
is impossible to determine.
increases....
asked 13 minutes ago -
The Baldwin Company currently has the following balances on their
balance sheet:
Total
Liabilities
$69,309
Common...
asked 16 minutes ago -
A quiet town in Kansas has 10 people, all of whom have the same
preferences. There...
asked 22 minutes ago -
Summarize what an organization needs from a leader.
a. Analyze what might happen to an organization...
asked 25 minutes ago -
How would one critically evaluate an organizations marketing
strategies from the viewpoint of its consumers, as...
asked 23 minutes ago -
Company XYZ know that replacement times for the quartz time
pieces it produces are normally distributed...
asked 39 minutes ago -
A) Write the acid-base reaction that occurs between Na2HPO4 and
NaOH
B) Write the possible reactions...
asked 52 minutes ago -
What advantages does the Natural Law Theory have in comparison
with the Divine Command Theory? Explain...
asked 58 minutes ago -
A diver comes off a board with arms straight up and legs
straight down, giving her...
asked 57 minutes ago