H12 Highlighted:

H10 Highlighted:

H14 Highlighted:

H11 Highlighted:

Wire Frame:

Into how many peaks would you expect the 1H NMR signals of the indicated protons to be split? (Assume all coupling constants are equal.) ball & stick + labels Highlight H12 Highlight H10 Highlight H14 Highlight H11 H12: H10: 2 H14: H11: Into how many peaks would you expect the "H NMR signals of the indicated protons to be split? (Assume all coupling constants are equal.) ball & stick - + labels Highlight H12 Highlight H10 Highlight H14 Highlight H11 Into how many peaks would you expect the "H NMR signals of the indicated protons to be split? (Assume all coupling constants are equal.) ball & stick - + labels Highlight H12 Highlight H10 Highlight H14 Highlight H11 Into how many peaks would you expect the "H NMR signals of the indicated protons to be split? (Assume all coupling constants are equal.) ball & stick - + labels Highlight H12 Highlight H10 Highlight H14 Highlight H11 Into how many peaks would you expect the "H NMR signals of the indicated protons to be split? (Assume all coupling constants are equal.) ball & stick - + labels Highlight H12 Highlight H10 Highlight H14 Highlight H11 How many electronically non-equivalent kinds of protons, and how many kinds of carbons are present in the following compound? (Don't forget that cyclohexane rings can undergo ring flips. ) ball & stick v- + labels a. kinds of protons: b. Kinds of carbons: (Don't forget that cyclohexane rings can undergo ring flips. ) H H M. wireframe + labels Propose a structure for a compound with the chemical formula C4H6 that shows only one peak in its 1H-NMR spectrum. . You do not have to consider stereochemistry. You do not have to explicitly draw H atoms. In cases where there is more than one answer, just draw one. aste . / [ ] ChemDoodle