The peak at 3.7 ppm is due to 4 Hs of two CH2 groups. They are diastereotopic to each other. Thats why each proton is splitted to multiplet and the signals combine with each other to give a complex pattern.
5. To which of the following molecules does the spectrum below belong? Explain your choice carefu...
Please assign all peaks and show work, thank you.
1. To which of the compounds below does the NMR spectrum shown below belong? Explain your answ carefully (1) cis-3-hexene (2) (Z)-1-ethoxy-1-butene (3) 2-ethyl-1-butene (5) CI,CH-CH(OCH2CH,2 200 100 0 8, ppm
5. Which of the molecule below gives the following 13C NMR spectrum? Explain your answer 200 300 BO 40 b) d) CHLECH.CH.CH, O -CH:CH-CH:CH HC HC CH.CH CH3CCH CH.CH 6. Which underlined hydrogen atom is the most deshielded? CHCH-CH3 (1) CH3OCHCH: (1) CICH:CH-CH3