1. IR – circle and label each type of bond present directly on the spectra. Label the type of bond each peak represents

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1. IR – circle and label each type of bond present directly on
the spectra. Label the type of bond each
peak represents (For example, instead of just saying alkane, you
could say C-H alkane, or Csp3-H).
2. 13C-NMR and 1H-NMR – Draw out the skeletal structure of the
compound, label the H’s a, b, c’s and
the C’s 1, 2, 3’s. Then label all signals on the NMR with those
corresponding letters/numbers.).
3. Please show your calculations for degrees of unsaturation and
integration ratios on one of the
previous handout pages in the margins.
*On each handout page please draw out the skeletal structure of
your unknown.

1 Ir Circle And Label Each Type Of Bond Present Directly On The Spectra Label The Type Of Bond Each Peak Represents 1 (32.21 KiB) Viewed 66 times

Transmittance 4000 -6 0 5 G880 8 8 8 8 8 8 8 3 3500 100 Mon Nov 27 20 28 04 2017 (GMT-07:00) 3000 Alkang C- 2984.71 2500 Wavenumbers (cm-1) 2000 Heron 1717.25 1646.39 144748 1500 146732 4368.00 Aromana c-c Steing 1394OZ 1293.77 1256.55 1175.53 1151.30 1224.86 1095 84 Isorening innown# 3 1031.45 977.45 1000 859.08 774 21 667.76 653 88

CHM 235LL-IR/NMR Techniques H NMR-UNKNOWN #3 C3H1204 E-0- P 80cm -CH₂-CH3 H3C - Hylo-c Srati CDC 06-300 C- 2 니 implies symmetry 2:46