Part I. Create a splitting tree diagram to predict the multiplet pattern of proton Hb in the compound below: 3 (Assume that "Jab >>> ³JbC) Ha Hb He он Ha NH2 Ha HC
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- Match each compound with the corresponding number of sets of equivalent protons. Compound A Compound B Compound C A) Compound D B) Drag and drop options on the right-hand side and submit. For keyboard navigation... SHOW MORE ✓ Br C) III ||| |||| = Br = 3 1 6 2 = 4 5 Br Br D) Oper2. Draw curved arrows that show the bond changes for each chemical step shown below. CH3 :: H3C e + H3C a) b) C X CH3 K+ :OH H3C CH3 + KI T: + H₂O2. Draw structures for compounds that have the proton nmrs described: a) C2H6O; one singlet b) CAH&Cl2O; two triplets c) CAHBO2; one singlet, one triplet and one quartet
- (a) Ph Br H HO CH3 713 A (b) HC- H HO H CH A Draw Newman projections looking down the indicated bond (right to left) representing the following compounds.9) For each compound shown below, convert the structure to zig-zag (line) notation. HO HO ČH3 H. (а) CH3CH2 CH3 H NH2 (b) Br YH ČH,CH2CH3How many different types of protons are present in each compound? (CH3)3CH 2. CH3CH2OCH2CH2CH2CH2CH3
- 2. Homework HelpPropose a structure consistent with each set of data.a. a compound that contains a benzene ring and has a molecular ion at m/z = 107b. a hydrocarbon that contains only sp3 hybridized carbons and a molecular ion at m/z = 84c. a compound that contains a carbonyl group and gives a molecular ion at m/z = 114d. a compound that contains C, H, N, and O and has an exact mass for the molecular ion at 101.0841H3C. H || IV Predict the correct splitting tree for circled hydrogen in the structure below. Br A) I B) II C) III D) IV
- k Please don't provide handwritten solutionDetermine the peak shape you would expect (singlet, doublet, triplet, quartet, etc) for each proton indicated with the arrow1. Provide an acceptable name for the following molecule. Only specify R and S where shown as 3D.: N3 N NO2 ОН SH H H Тext Br H,N NH2
