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) A compound with molecular formula CxH 1403 displays the following spectral data. Propose a structure...
Use the spectral data provided to determine the structure of the following organic conpounds. IR Spectrum...
Use the spectral data provided to determine the structure of
the following organic conpounds.
IR Spectrum ouid im) 3410 4000 3000 2000 1600 1200 V (om: 800 100 Mass Spectrum 43 80 60 M (15) 71 20 40 120 80 160 200 240 280 m/e 13C NMR Spectrum (50.0 M, COCI, solution) DEPT CHt CH,t CHt solvent proton decoupled 0 8 (ppm) 40 80 120 200 160 'H NMR Spectrum (200 MHz, CDCI, solution) expansion exchanges with Dy0 50 pom...
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...
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,...
5. The spectral data provided below are for a compound with a molecular weight of 1 94 g/mol. Outline your interpre...
5. The spectral data provided below are for a compound with a molecular weight of 1 94 g/mol. Outline your interpretation of the data in point form and from your points, propose a structure consistent with the spectral data provided IR Spectrum (quid fim) 1712 1277 1254 L.... 800 2000 1600 V (cm) 1200 4000 3000 C NMR Spectrum Resolves into two signals at higher feld solvent proton decoupled o 8(ppm) 160 120 80 40 200 H NMR Spectrum (200...
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 6 1756 IR Spectrum uid Sm) 15820 4000 3000 2000 1600 1200 800 V (cm) 100 55 Mass Spectrum 71 80 70 60 No significant UV M158 (1%) absorption above 220 nm C&H140s 40 80 120 160 200 240 280 m/e 13C NMR Spectrum (50.0 MHz,...
Identify the structure Problem 120 mm IR Spectrum liquid film) 1734 4000 3000 2000 1200 800...
Identify the structure
Problem 120 mm IR Spectrum liquid film) 1734 4000 3000 2000 1200 800 1600 V (cm) 100 Mass Spectrum M 128 80 60 40F wodowe No significant UV absorption above 220 mm 83 100 113 C-H1202 40 80 120 200 240 280 160 m/e 13C NMR Spectrum (100.0 MHZ. CDCI, solution) DEPT Chat Chat Cht W proton decoupled 200 160 120 80 40 O 8 (ppm) H NMR Spectrum (400 MHE, COCI, solution) expansions oppm 1936 ppi...
Q-2……………..By identifing the sprectra provide the information about the structure , Please provide the structure of...
Q-2……………..By
identifing the sprectra provide the information about the structure
, Please provide the structure of the compound. Justification (i.e.
shifts, multiplicities, peaks etc.) for your structure should be
given.
13C NMR Spectrum (100.0 MHz, CDCI, solution) DEPT CH CH. CH 3395 solvent proton decoupled IR Spectrum liquid film) 1093 LLLLLLLLLLLL 20016012080 400 g (ppm) 4000 3000 2000 V (cm 800 1600 ) 1200 expansion expansions TH NMR Spectrum (400 MHz, CDCI, solution) 91 107 Mass Spectrum expansion 5.14 5.10...
BONUS (10 pts) Determine the compound structure based on the spectra below. Annotate spectra to receive...
BONUS (10 pts) Determine the compound structure based on the spectra below. Annotate spectra to receive full credit 3457 IR Spectrum (CHCI solution) 4000 3000 2000 V (cm 1600 ) 1200 800 Mass Spectrum TY of base peak UV Spectrum 2 max 263 nm (1090€ 3.9) 2 max 305 nm (10910€ 2.1) solventi hexane 40 80 200 240 280 120 160 m/e Q Search BC NMR Spectrum (100.0 MH, CDC, solution) DEPT CH CH cht profon decoupled 200 8 (ppm)...
Deduce the structure of the following 7 compounds given their IR, 'H NMR, and 13C NMR...
Deduce the structure of the following 7 compounds given their IR, 'H NMR, and 13C NMR spect ra, and draw their structure in the space provided below. For full credit, assign IR functional group absorptions and assign the structure's protons and carbons to their respective spectral resonances. For questions 8-10, provide a step- by-step mechanism for the transformations shown. The quiz must be turned in at the beginning of class on Wednesday, November 20, 2019 Compound 6: C$H14O3 Compound 6...
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...
Use the spectral data provided to determine the structure of
the following organic conpounds.
IR Spectrum ouid im) 3410 4000 3000 2000 1600 1200 V (om: 800 100 Mass Spectrum 43 80 60 M (15) 71 20 40 120 80 160 200 240 280 m/e 13C NMR Spectrum (50.0 M, COCI, solution) DEPT CHt CH,t CHt solvent proton decoupled 0 8 (ppm) 40 80 120 200 160 'H NMR Spectrum (200 MHz, CDCI, solution) expansion exchanges with Dy0 50 pom...
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...
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,...
5. The spectral data provided below are for a compound with a molecular weight of 1 94 g/mol. Outline your interpretation of the data in point form and from your points, propose a structure consistent with the spectral data provided IR Spectrum (quid fim) 1712 1277 1254 L.... 800 2000 1600 V (cm) 1200 4000 3000 C NMR Spectrum Resolves into two signals at higher feld solvent proton decoupled o 8(ppm) 160 120 80 40 200 H NMR Spectrum (200...
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 6 1756 IR Spectrum uid Sm) 15820 4000 3000 2000 1600 1200 800 V (cm) 100 55 Mass Spectrum 71 80 70 60 No significant UV M158 (1%) absorption above 220 nm C&H140s 40 80 120 160 200 240 280 m/e 13C NMR Spectrum (50.0 MHz,...
Identify the structure
Problem 120 mm IR Spectrum liquid film) 1734 4000 3000 2000 1200 800 1600 V (cm) 100 Mass Spectrum M 128 80 60 40F wodowe No significant UV absorption above 220 mm 83 100 113 C-H1202 40 80 120 200 240 280 160 m/e 13C NMR Spectrum (100.0 MHZ. CDCI, solution) DEPT Chat Chat Cht W proton decoupled 200 160 120 80 40 O 8 (ppm) H NMR Spectrum (400 MHE, COCI, solution) expansions oppm 1936 ppi...
Q-2……………..By
identifing the sprectra provide the information about the structure
, Please provide the structure of the compound. Justification (i.e.
shifts, multiplicities, peaks etc.) for your structure should be
given.
13C NMR Spectrum (100.0 MHz, CDCI, solution) DEPT CH CH. CH 3395 solvent proton decoupled IR Spectrum liquid film) 1093 LLLLLLLLLLLL 20016012080 400 g (ppm) 4000 3000 2000 V (cm 800 1600 ) 1200 expansion expansions TH NMR Spectrum (400 MHz, CDCI, solution) 91 107 Mass Spectrum expansion 5.14 5.10...
BONUS (10 pts) Determine the compound structure based on the spectra below. Annotate spectra to receive full credit 3457 IR Spectrum (CHCI solution) 4000 3000 2000 V (cm 1600 ) 1200 800 Mass Spectrum TY of base peak UV Spectrum 2 max 263 nm (1090€ 3.9) 2 max 305 nm (10910€ 2.1) solventi hexane 40 80 200 240 280 120 160 m/e Q Search BC NMR Spectrum (100.0 MH, CDC, solution) DEPT CH CH cht profon decoupled 200 8 (ppm)...
Deduce the structure of the following 7 compounds given their IR, 'H NMR, and 13C NMR spect ra, and draw their structure in the space provided below. For full credit, assign IR functional group absorptions and assign the structure's protons and carbons to their respective spectral resonances. For questions 8-10, provide a step- by-step mechanism for the transformations shown. The quiz must be turned in at the beginning of class on Wednesday, November 20, 2019 Compound 6: C$H14O3 Compound 6...
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...
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