ts of alkenes only (g) Calculate the % yield of the products Part B:Complete Table 3...

Question

Question

Answer 1

Answer #1

The reaction taking place in the flask is dehydration of 2-methyl cyclohexanol which can be explained by the following chemical equation:

OH CH3 CH3 .CH3 phosphoric acid H2SO major product minor product Hoffman product Zaitsev product

The formation of the product is confirmed by the bromine test which explains the addition of bromine to the double bond.

The KMnO₄ test also confirms the product formation

In th IR spectrum, The C-H stretching vibrations attached to the C=C double bond at 2921cm^-1 explains the formation of the product.

Answer 2

Similar Homework Help Questions

report 13 C NMR, DEPT, observed bp. Evidence should be given that shows the reaction yeilded...

report 13 C NMR, DEPT, observed bp. Evidence should be given that shows the reaction yeilded an ester product. Specific evidenceshould be given to support the identification of the product ester and starting alcohol. find the starting alcohol and state product ester Compare the IR spectrum to the IR spectrum of the starting material. Assign all the major peaks above the fingerprint region in your IR spectra. Assign the signals in the carbon and Dept NMR spectra. what evidence do...
using the IR, the 13C, and DEPT NMR spectra of your product determine the identity of...

using the IR, the 13C, and DEPT NMR spectra of your product determine the identity of your unknown ester from a C-4 or C-5 alcohol. the identity of the C-4 or C-5 alcohol also needs to be determined. The following C-4 or C-5 alcohols will be used in this experiment: 1-butanol (n-butyl alcohol) 2-butanol (sec-butyl alcohol) 2-methyl-1-propanol (isobutyl alcohol) 3-methyl-1-butanol (isopentyl alcohol) 1-pentanol (n-pentyl alcohol) 2-pentanol 3-pentanol cyclopentanol Questions: 1. Why is the mixture extracted with aqueous sodium bicarbonate solution?...