Use the spectra below to answer for K and O
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Use the spectra below to answer for K and O Show the synthesis of Kt o...
Show the synthesis from acetylene for K (C11 H14 O) and O (C5
H12 O) using the spectra below
Molecule 1 Molecule O Molecule K ЗН 3H 5H 2H diastereotopic 1н PPM o Molecule O 6H 4H 1H 1H exchangeable PPM
Use the spectra above to determine the reactions and the
products of K, and O
Answer in the boxes below
Reactions
Products
Syaimin tg Kio fmи аеyene adyene РАРТ Show Yu SprTHEGNS CuHMO CsHO Molecule K ЗН 3H 5H 2H diastereotopic 1н PPM o Molecule O 6H 4H 1H 1H exchangeable PPM K O К O
Compound 2: Use the information provided below and the IR and NMR spectra on the next page to answer the following questions. a) An MS was taken of compound 2 and the table is given below. Determine the molecular formula of 2 from the MS given below relative abundance m/z 132 100 133 9.8 b) Calculate the Index of Hydrogen Deficiency/Degree of Unsaturation for the molecule. c) Using the IR spectrum and the 1H- and 13C-NMR spectra given below, determine...
Use the spectra below to fill in all the letter spaces in the
Guided synthesis
Molecule 9H Зн 2н 2н PPM Molecule ) 9H ЗН ін 2H 2H Е - Molecule F IH L6H 2H2H Clotis 1. Imole Hel 1.Li/NH3 -78°c 2. Mc PBA 2. 1 mole HI Kamaryu H NMR/IR VE c) H₂O FNne) (NMR/IR lCq H180 co ter) C10Hz, Br
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8.8 Identify the compounds of the given molecular formulas that show a. One 'H NMR signal: CHO CH C.H.Br, b. Two 'H NMR signals: CH.CL CHO CHO, CHOCI 8.9 8.10 How many 'H NMR signals will each of the compounds below show? a. (CH, CHỊCH, d. CH.COCH,CH.COCH, b. CH,COCOOCH, e. CH.COCH.CH.COOCH, c. CH,COCH,COCH, L. CHCOCH CH(CI)COCH, Suggest structures consistent with the following 'H NMR data: а. Сно CHCI triplet (1.0 ppm, 3H)...
Use the spectra below to fill in the boxes for the reaction
above.
If it isn't clear box J is (C11 H24 O) and box I is (C9 H10
O)
NARCC H240) NMR (Cq HOO) Molecule 9H Зн 2н 2н PPM Molecule ) 9H ЗН ін 2H 2H Е -
Below is the H NMR spectra for the molecule styrene.
Consider if a hydroboration reaction was preformed on styrene.
How would the H NMR of the expected product change in comparison to
styrene? Circle which peaks from the styrene spectra would
disappear and not be present in the NMR of the product.
Draw the expected product. Describe the splitting pattern of
each new proton signal that would appear in the NMR of the
product.
2) Below is the 'H NMR...
Use the spectra above to fill in the letter spaces in the guided
synthesis.
Clotis 1. Imole Hel 1.Li/NH3 -78°c 2. Mc PBA 2. 1 mole HI Kamaryu H NMR/IR VE c) H₂O FNne) (NMR/IR lCq H180 co ter) C10Hz, Br Molecule 9H Зн 2н 2н PPM Molecule ) 9H ЗН ін 2H 2H Е - Molecule F IH L6H 2H2H
Use the spectra above to fill in the letter spaces in the guided
synthesis in the boxes below
Clotis 1. Imole Hel 1.Li/NH3 -78°c 2. Mc PBA 2. 1 mole HI Kamaryu H NMR/IR VE c) H₂O FNne) (NMR/IR lCq H180 co ter) C10Hz, Br Molecule 9H Зн 2н 2н PPM Molecule ) 9H ЗН ін 2H 2H Е - Molecule F IH L6H 2H2H We were unable to transcribe this imageWe were unable to transcribe this imageWe were unable...
Compound 3: Use the information provided below and the IR and NMR spectra on the next page to answer the following questions. a) An MS was taken of compound 3 and the table is given below. Determine the molecular formula of 3 from the MS given below. . relative abundance m/z 152 100 153 9.7 154 4.5 b) Calculate the Index of Hydrogen Deficiency/Degree of Unsaturation for the molecule. c) Using the IR spectrum and the 'H- and 13C-NMR spectra...