choose the correct structure for the compound whose nmr is shown below X3 Q10 G6 Choose...
Choose the correct structure for the product of the following reaction Towe O A A OBB O Cc D D a Save Unanswered X3 Q10 G8 Choose the correct structure for the compound with the nmr shown Chemical Formula: CHO
Shown above is the 1H-NMR spectrum of a compound with the formula C5H10O2 . Choose from the constitutional isomers below to assign a structure to this spectrum. 3H 2H 3H 2H PPM Shown above is the 'H-NMR spectrum of a compound with the formula C5Hi002. Choose from the constitutional isomers below to assign a structure to this spectrum a b C CH3CH2CH2CH2COH CH3CH2COCH2CH3 CH3CH2CH2COCH3 (Choose the letter corresponding to the correct structure from the drop-down list provided.) Correct Structure: Assign...
Choose the correct structure for the compound with the nmr shown Chemical Formula: C,H,O, O A A o BB o CC ODD Unanswered a save a Save
4 (10 pts) 7. Determine the structure of compound C, whose NMR is shown below. The formula for C is CH,CI. The IR has a band at 2950 cm. Assign the NMR signals to the structure you are proposing (i.e. label your hydrogens). Alkene Compound C GHA 2HE 2WE 2HD IRC 0.14 0.15 0.07 0.15 0.43 PPM
Draw the structure of the compound whose molecular formula is C9H10O and has the following proton NMR data: Draw the structure of the compound whose molecular formula is C9H100 and has the following proton NMR data: triplet at 1.2 ppm, integrates to 3H quartet at 2.7 ppm, integrates to 2H doublet at 7.3 ppm, integrates to 2H doublet at 7.7 ppm, integrates to 2H singlet at 9.9 ppm, integrates to 1H Take a photo of your answer and upload it...
she major 4. Draw the correct structure for the compound with the nmr shown below which leads by Claisen rearrangement to the structure shown CH10 stify th one pode ually w ndered bescher wa cler 2H 2H Claisen Rearrangement Product
The H-NMR spectrum of an unknown compound (formula CaHgO2) is shown below. Draw the structure of the unknown compound. Question 5 4 1 6 5 8 10 11 Ppm The 13C-NMR spectrum of an unknown compound (formula CgH180) is shown below. Its 1H-NMR spectrum only shows one singlet at 1.2 ppm. Draw the structure of this unknown compound. uestion 2 220 200 160 140 120 PPM 100 80 240 180 60 40 20 Create OscerSketch Answer 2 What would be...
Daw the structure that gives the NMR below. The compound has the more e NMR below. The compound has the molecular formula, C5H1002. Signal at 4.13 (triplet, 2H), 2.04 (singlet, 3H), 1.73 (sextet, 2H) and shows strong bands at 1710 cm (Singlet, 3H), 1.73 (sextet, 2H) and 1.01 (triplet, 3H). IR and 1200 cm (in addition to others). Make sure to indicate (label) which hydrogen gives which signal PPM
4. Determine the structure of an unknown compound whose mass, IR, and 'H-NMR spectra are shown below.. MS 100 43 71 Structure of the unknown compound 50 114 0 40 60 80 100 120 m/z IR H-NMR δ (ppm) 0
1H NMR 6. Propose a structure for the compound CzH.O with the following 'H NMR spectral data. 2H 1H 3H 1110 H ppm 7. Propose a structure for the compound C2H60, with the following 'H NMR spectral data. (Note this is the same molecular formula as the previous question) ppm 8. Propose a structure for the compound C,He with the following 'H NMR spectral data. SH2H 1H ppm 9. Propose a structure for the compound CxHyN with the following 'H...