Can someone explain 2E the question is asking and this is what my professor said but I am lost as heck now please help here is the question: Can you also check 2 D as well. Q: Provide the reagents needed to carry out the reactions below (or the product obtained). If two steps are needed, clearly indicate 1. (reagent A); 2. (reagent B). If separate steps are not indicated, I will assume you mean that all reagents are introduced together. dou ble bonastundeesring1. HzSoyladdsdouble bond)2.H20i OH Coldd)OHHO.·Azo,-0H sini Jar toHOmC PBA, PlacesOH groußs wish SameSterochenist.OHTsCle)gets rid of OH, hrden. Treatment of an alcohol with tosylchloride converts the alcohol to a tosylate ester (a"tosylate," the "OTs group). That's a good leavinggroup, and it can be an entry point for differentsubstitution and elimination reactions. The questionis what do you want to do with the tosylate?Substitute with something? Perform an eliminationto generate a double bond?In the end, you need to wind up with a hydrocarbon.What reactions have you seen that have simplehydrocarbons as products?

The question is based on the concept of organic reactions. we have to identify the reagents…

Answered: d) 2. H20i OH Cold HO, mC PRA, Places…

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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Can someone explain 2E the question is asking and this is what my professor said but I am lost as heck now please help here is the question: Can you also check 2 D as well.

Q: Provide the reagents needed to carry out the reactions below (or the product obtained). If
two steps are needed, clearly indicate 1. (reagent A); 2. (reagent B). If separate steps are not indicated, I will assume you mean that all reagents are introduced together.

dou ble bonas
tundeesring
1. HzSoyladds
double bond)
2.H20i OH Cold
d)
OH
HO.
·Azo,-0H sini Jar to
HO
mC PBA, Places
OH groußs wish Same
Sterochenist.
OH
TsCl
e)
gets rid of OH,

hrden. Treatment of an alcohol with tosyl
chloride converts the alcohol to a tosylate ester (a
"tosylate," the "OTs group). That's a good leaving
group, and it can be an entry point for different
substitution and elimination reactions. The question
is what do you want to do with the tosylate?
Substitute with something? Perform an elimination
to generate a double bond?
In the end, you need to wind up with a hydrocarbon.
What reactions have you seen that have simple
hydrocarbons as products?

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