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PPM 1.(5 pts) Draw the structure of the substituted benzene that forms instead AND label the...
please draw the structure 1-hexanol and label all the H atoms on the structure corresponding to...
please draw the structure 1-hexanol and label all the H atoms on
the structure corresponding to the peaks below in the H NMR
spectrum.
TEHO Common Name: 'H NMR IUPAC Name: Zoom Out CAS No.: Solvent: BP: MP: 1.00 0.90 0.80 0.70 0.60 0.50 0.40 0.30 0.20 0.10 0.001 1.0 4.0 No. Height No Height 11655 Height Height 1 Height 44.465 81.003 323 24 No. 4 5 6 3.0 No. 7 8 9 2.0 No. 13 14 15 OK SAVE...
QUESTIONS 1. NMR (2 Points) Draw the structure of acetaminophen and label chemically-equivalent hydrogen atoms with...
QUESTIONS 1. NMR (2 Points) Draw the structure of acetaminophen and label chemically-equivalent hydrogen atoms with the same lowercase letter. a. b. (2 Points) Find the peaks that represent these protons on the NMR spectrum of Tylenol, and write down the chemical shift of those peaks next to the protons you labeled nu differences in the peaks in the Excedrin and Tylenol
2. Draw the structure of the major organic product that is formed from the following reaction....
2. Draw the structure of the major organic product that is formed from the following reaction. Draw this structure in the box at the bottom of the next page. Then use letters to label all the sets of chemically equivalent carbons in this structure. The broadband proton-decoupled 13C NMR spectrum of the product is shown below. DEPT 90 and DEPT 135 data are included in the table on the following page. Use this spectroscopic data to make clear assignments of...
cvg.c owLv2 1 Onine and from Draw the structure of the compound CHio that exhibits the...
cvg.c owLv2 1 Onine and from Draw the structure of the compound CHio that exhibits the "C-NMR spectrum below. Impurity peaks are omitted from the peak list. The triplet at 77 ppm is CDCI Ueed wth permissicn from Aidrch Chemieal Co Ire Shift 1442 1283 27.8 125.5 28.9 15.6 Chemical shift: 1872 149.5 11.7 73.9 362 1.8 Chemical shift, δ (ppm) . You do not have to consider stereochemistry . You do not have to explicitly draw H atoms. ....
1. In the H NMR, draw the structure of the molecule directly on the spectrum and...
1. In the H NMR, draw the structure of the molecule directly on
the spectrum and identify each unique proton. Indicate which proton
is responsible for each peak.
2. In the IR spectrum, indicate which functional group is
responsible for each important peak. Attempt to identify at least
five important peaks. In you discussion, indicate which peaks are
most helpful in determining whether or not you converted the
starting material to the desired product.
3. Compare the IR spectrum of...
What is answer of #10?? Report: Hydroboration of 1-Methylcyclohexene Mechanism / GC Analysis / Calculations 1....
What is answer of #10??
Report: Hydroboration of 1-Methylcyclohexene Mechanism / GC Analysis / Calculations 1. After reviewing the GC and 'H NMR spectra, what is the major product of the reaction? + 3 a. BH: . THF 3 b. 3 H2O2 OH + 3 OH c. NaOH MOH OH racemic racemic major 2. Draw the complete curved arrow mechanism for the reaction to produce the major product, including both the hydroboration and oxidation steps. Repetitive steps need only be...
please need help with all the questions and ASAP, thank you 11. Please predict the principle...
please need help with all the questions and ASAP, thank you
11. Please predict the principle organic product of the following reactions, show stereochemistry where appropriate. Note that some reactions involve isotope-labeled compounds, in those cases the correct isotope must be used. (66') 1. LIAID 2. H,O (1) 18 1) THF (2). CH3Li + 2) HaO NaBH4 (3) CH3OD H2(excess)/Pt (4) d herd (5). - Mg Br D2O diethyl ether Br +Li (6) diethyl ether LICu(CH2CHs)2 Br (7). 1. diethyl...
What is answer of #9??? Help me Report: Hydroboration of 1-Methylcyclohexene Mechanism / GC Analysis /...
What is answer of #9???
Help me
Report: Hydroboration of 1-Methylcyclohexene Mechanism / GC Analysis / Calculations 1. After reviewing the GC and 'H NMR spectra, what is the major product of the reaction? + 3 a. BH: . THF 3 b. 3 H2O2 OH + 3 OH c. NaOH MOH OH racemic racemic major 2. Draw the complete curved arrow mechanism for the reaction to produce the major product, including both the hydroboration and oxidation steps. Repetitive steps need...
What is answer of #6??? Lab Section: 0 2 Report: Hydroboration of 1-Methylcyclohexene Mechanism / GC...
What is answer of #6???
Lab Section: 0 2 Report: Hydroboration of 1-Methylcyclohexene Mechanism / GC Analysis / Calculations 1. After reviewing the GC and 'H NMR spectra, what is the major product of the reaction? a. BHS. THF, OH O a. BH3. THE OH + b. 3 H2O2 3 + 3 c. NaOH OH ОН racemic racemic major 2. Draw the complete curved arrow mechanism for the reaction to produce the major product, including both the hydroboration and oxidation...
Please help with questions 1-5. I have attached the additional lab information pages for help if...
Please help with questions 1-5. I have attached the additional
lab information pages for help if you are unclear on anything
please review those.
We were unable to transcribe this imageEAS 97 5. Calculate the theoretical yiel te the theoretical yield of iodinated salicylamide (product) ass Todination reaction. (Show your calculations.) mide (product) assuming a mono- le, your starting material, is shown in Figure 4. ces in the functional group region of the spectrum IR spectrum of salicylamide, your starting...
please draw the structure 1-hexanol and label all the H atoms on
the structure corresponding to the peaks below in the H NMR
spectrum.
TEHO Common Name: 'H NMR IUPAC Name: Zoom Out CAS No.: Solvent: BP: MP: 1.00 0.90 0.80 0.70 0.60 0.50 0.40 0.30 0.20 0.10 0.001 1.0 4.0 No. Height No Height 11655 Height Height 1 Height 44.465 81.003 323 24 No. 4 5 6 3.0 No. 7 8 9 2.0 No. 13 14 15 OK SAVE...
QUESTIONS 1. NMR (2 Points) Draw the structure of acetaminophen and label chemically-equivalent hydrogen atoms with the same lowercase letter. a. b. (2 Points) Find the peaks that represent these protons on the NMR spectrum of Tylenol, and write down the chemical shift of those peaks next to the protons you labeled nu differences in the peaks in the Excedrin and Tylenol
2. Draw the structure of the major organic product that is formed from the following reaction. Draw this structure in the box at the bottom of the next page. Then use letters to label all the sets of chemically equivalent carbons in this structure. The broadband proton-decoupled 13C NMR spectrum of the product is shown below. DEPT 90 and DEPT 135 data are included in the table on the following page. Use this spectroscopic data to make clear assignments of...
cvg.c owLv2 1 Onine and from Draw the structure of the compound CHio that exhibits the "C-NMR spectrum below. Impurity peaks are omitted from the peak list. The triplet at 77 ppm is CDCI Ueed wth permissicn from Aidrch Chemieal Co Ire Shift 1442 1283 27.8 125.5 28.9 15.6 Chemical shift: 1872 149.5 11.7 73.9 362 1.8 Chemical shift, δ (ppm) . You do not have to consider stereochemistry . You do not have to explicitly draw H atoms. ....
1. In the H NMR, draw the structure of the molecule directly on
the spectrum and identify each unique proton. Indicate which proton
is responsible for each peak.
2. In the IR spectrum, indicate which functional group is
responsible for each important peak. Attempt to identify at least
five important peaks. In you discussion, indicate which peaks are
most helpful in determining whether or not you converted the
starting material to the desired product.
3. Compare the IR spectrum of...
What is answer of #10??
Report: Hydroboration of 1-Methylcyclohexene Mechanism / GC Analysis / Calculations 1. After reviewing the GC and 'H NMR spectra, what is the major product of the reaction? + 3 a. BH: . THF 3 b. 3 H2O2 OH + 3 OH c. NaOH MOH OH racemic racemic major 2. Draw the complete curved arrow mechanism for the reaction to produce the major product, including both the hydroboration and oxidation steps. Repetitive steps need only be...
please need help with all the questions and ASAP, thank you
11. Please predict the principle organic product of the following reactions, show stereochemistry where appropriate. Note that some reactions involve isotope-labeled compounds, in those cases the correct isotope must be used. (66') 1. LIAID 2. H,O (1) 18 1) THF (2). CH3Li + 2) HaO NaBH4 (3) CH3OD H2(excess)/Pt (4) d herd (5). - Mg Br D2O diethyl ether Br +Li (6) diethyl ether LICu(CH2CHs)2 Br (7). 1. diethyl...
What is answer of #9???
Help me
Report: Hydroboration of 1-Methylcyclohexene Mechanism / GC Analysis / Calculations 1. After reviewing the GC and 'H NMR spectra, what is the major product of the reaction? + 3 a. BH: . THF 3 b. 3 H2O2 OH + 3 OH c. NaOH MOH OH racemic racemic major 2. Draw the complete curved arrow mechanism for the reaction to produce the major product, including both the hydroboration and oxidation steps. Repetitive steps need...
What is answer of #6???
Lab Section: 0 2 Report: Hydroboration of 1-Methylcyclohexene Mechanism / GC Analysis / Calculations 1. After reviewing the GC and 'H NMR spectra, what is the major product of the reaction? a. BHS. THF, OH O a. BH3. THE OH + b. 3 H2O2 3 + 3 c. NaOH OH ОН racemic racemic major 2. Draw the complete curved arrow mechanism for the reaction to produce the major product, including both the hydroboration and oxidation...
Please help with questions 1-5. I have attached the additional
lab information pages for help if you are unclear on anything
please review those.
We were unable to transcribe this imageEAS 97 5. Calculate the theoretical yiel te the theoretical yield of iodinated salicylamide (product) ass Todination reaction. (Show your calculations.) mide (product) assuming a mono- le, your starting material, is shown in Figure 4. ces in the functional group region of the spectrum IR spectrum of salicylamide, your starting...
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