Predict the splitting patterns you would expect for each proton in the molecules below. c. doublet a. septet H CH3 b. singlet d. quartet C1 H

What are the configurations of the two stereogenic carbon atoms in this molecule? CI H 5 6 O 3 2 4 H3C H A. (3R, 6R) B. (3R, 6S) OC. (3S, 6R) OD. (3S, 6S)

2. Determine the absolute configuration (R/S) of the molecules below. CI H NH,

Propanal (bp 48°C) and propanol (bp 97°C), both found on Table 4.2, have very similar surfaceareas and dipole moments. Construct an explanation for the large difference in boiling pointsbetween the two.

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Name the compunds and identify the RS configuration

1. What is the absolute configuration of the molecule shown? H OH за b. H CH да НО-С OH HỌC CHI CH •H .COH OH

Indicate the expected splitting for the protons in the structures like: singlet, doublet, triplet of quartets or other for eachI needed help doing this for A, B, C, and D that are shown in the picture I submited. Can someone help and explain?

Which molecule has the greatest number of unique protons? How many unique protons does each molecule have?

LI H Br 'к The molecule from question 2 is shown above with an S-configuration. Identify any of the following represenations of th esame molecule that also have the S-configuration. Choose all that apply. 000 FEB 19 Get the mobile app A K B Br LISO Br you с tv S O Finish attempt....