Chemistry
Chemistry, 16.08.2021 22:40, OnlineSchool

Compound A has molecular formula C7H140 and reacts with sodium borohydride in methanol to form an alcohol. The 1H NMR spectrum of compound A exhibits only two signals: a doublet (I12) and a septet (2). Treating compound A with 1,2-ethanedithiol (HSCH2CH2SH) followed by Raney nickel gives compound B. (a) How many signals will appear in the 1H NMR spectrum of compound B?
(b) How many signals will appear in the 13c NMR spectrum of compound B?
(c) Complete the description of how you could use IR spectroscopy to verify the conversion of compound A to compound B. Compound A is a 1, while compound B is an. Therefore, Compound A exhibit a signal at approximately 1715 cm, while compound B exhibit a signal in the same region.

answer
Answers: 2

Other questions on the subject: Chemistry

image
Chemistry, 22.06.2019 13:10, mallyosburn
Draw two cyclic constitutional isomers of cis-1
Answers: 2
image
Chemistry, 23.06.2019 02:30, ijustneedhelp29
Which of the following statements are incorrect?
Answers: 3
image
Chemistry, 23.06.2019 03:30, cupcake3103670
Name 3 types of energy you see being used as you look around a classroom
Answers: 1
image
Chemistry, 23.06.2019 04:10, xojade
In an experiment, 45g of silicon tetrachloride are treated with 45ml of water. what is the theoretical yield in grams of hcl
Answers: 3
Do you know the correct answer?
Compound A has molecular formula C7H140 and reacts with sodium borohydride in methanol to form an al...

Questions in other subjects:

Konu
Mathematics, 13.02.2021 18:00
Konu
Mathematics, 13.02.2021 18:00