with detail mechanism ( do i 2. (a) Predict the product(s) of the followingplausiblereactionmechanisms :andsuggest1) Δ or hw(i)>?2) 5% КОН, ЕtОНČIOTfPd(PPH3)4(5 mol%)→?(ü)+ BnSnLiCl, THFCH3CH2OH(iüi)DCC→?DMAPСООН

The question First is an example of Hoffman Loffler Freytag reaction.

Answered: (a) Predict the product(s) of the…

(a) Predict the product(s) of the following plausible reaction and suggest mechanisms : (i) 1) A or hv →? 2) 5% KOH, EtOH

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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Give clear detailed mechanism Solution with explanation needed..don't give Handwritten answer
UPVOTE WILL BE GIVEN. PLEASE ANSWER IT CORRECTLY. NO LONG EXPLANATION NEEDED.
give the proper mechanism
Give detailed mechanism Solution with explanation needed..don't give Handwritten answer
Product and reaction mechanism?
Edit View History ALEKS = F Bookmarks 2 Explanation W X O SUBSTITUTION REACTIONS Understanding how the degree of substrate substitution... >> www-awu.aleks.com/alekscgi/x/Isl.exe/1o_u-IgNslkr7j8P3jH-liGBdp5ulp5VqUnMDyPOVaX6q0CRPLZSQ5NeitEiCEgQdufl52nFL-pi0arA2XzDPmO... 3 # Profiles Check E You want to replace all the Br atoms in the following molecule with hydroxy (OH) groups, and you know there are two competing mechanisms by which this reaction can occur: Tab ALEKS - Tiffany Te-L-Peng - L X Mechanism 1: A nucleophile can replace the Br atom in a concerted, bimolecular step. Highlight in red the Br atom that would be replaced quickest if the reaction went by this type of mechanism. Mechanism 2: A nucleophile can replace the Br atom in several steps, the slowest of which is unimolecular. Highlight in blue the Br atom that would be replaced quickest if the reaction went by this type of mechanism. If you would highlight the same Br atom for both mechanisms, highlight it in green instead.…
File Edit View History Bookmarks Profiles Tab Window Help ● с ALEKS O SUBSTITUTION REACTIONS Understanding how the degree of substrate substitution... www-awu.aleks.com/alekscgi/x/lsl.exe/10_u-IgNslkr7j8P3jH-liGBdp5ulp5VqUnMDyPOVaX6q0CRPLZSQ5Ne1rzjYfhTzHbIRMe2EN-ukW4SrUeFejsT... Explanation @ ALEKS - Tiffany Te-L-Peng - L X + → You want to replace all the CI atoms in the following molecule with hydroxy (OH) groups, and you know there are two competing mechanisms by which this reaction can occur: # Check Mechanism 1: A nucleophile can replace the Cl atom in several steps, the slowest of which is unimolecular. Highlight in red the CI atom that would be replaced quickest if the reaction went by this type of mechanism. Mechanism 2: A nucleophile can replace the Cl atom in a concerted, bimolecular step. Highlight in blue the Cl atom that would be replaced quickest if the reaction went by this type of mechanism. If you would highlight the same Cl atom for both mechanisms, highlight it in…
For indicated reaction provide: Ionic polymerization of propene. a. general equationb. Mechanismc. Discussion of regioselectivityd. Discussion of the proportion between the products formed (if more than one is formed).e. Discussion of stereoselectivity.
please provide mechanism
GIVE PRODUCT WITH MECHANISM DO ALL VERY EASY QUESTION , IF U PLAN TO DO ONLY 1 OR 2 THEN , SKIP SOMEONE WILL DO ALL
Give detailed mechanism Solution with explanation needed. don't give Handwritten answer
Provide a mechanism