Calculate the theoretical yield for the reaction based on 2.0g of 2-methyl-3-pentanol (MW= 102.18g/mol) and 2.0 mL of the 48%HBr -(show calculatins for both reactions ) -molecular weight of product must be determined based on the structure-identify theoretical yeild on the limiting reagent. * OH is a bad learingerup $ needs to be pronatedto Hzo fer the sor to proceed!HBKeeThis is anexanmple of 1st order nucleophilicsubstitution rxn.mechanism:Glaw)ratedet-ster主2° COOH2intermediaterearangemntproduct #1(mincr)3-Bromo-2-methylßentare.or3° COmere stableintermediateBrproduct #2(majar) blc3° CO is mre.Stalde than 2° CO2-Bromo-2-methylpantane.PRODUCTS!

From given mechanism we can determine molecular weight and theoretical yield is calculated as…

Calculate the theoretical yield for the reaction based on 2.0g of 2-methyl-3-pentanol (MW= 102.18g/mol) and 2.0 mL of the 48%HBr -(show calculatins for both reactions ) -molecular weight of product must be determined based on the structure -identify theoretical yeild on the limiting reagent.

Calculate the theoretical yield for the reaction based on 2.0g of 2-methyl-3-pentanol (MW= 102.18g/mol) and 2.0 mL of the 48%HBr -(show calculatins for both reactions ) -molecular weight of product must be determined based on the structure -identify theoretical yeild on the limiting reagent.

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter17: Alcohols And Phenols

Section17.SE: Something Extra

Problem 60AP: Benzvl chloride can be converted into benzaldehvde by treatment with nitromethane and base. The...

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Question

Calculate the theoretical yield for the reaction based on 2.0g of 2-methyl-3-pentanol (MW= 102.18g/mol) and 2.0 mL of the 48%HBr -(show calculatins for both reactions )

-molecular weight of product must be determined based on the structure

-identify theoretical yeild on the limiting reagent.

* OH is a bad learing
erup $ needs to be pronated
to Hzo fer the sor to proceed!
HBK
ee
This is anexanmple of 1st order nucleophilic
substitution rxn.
mechanism:
Glaw)
rate
det-ster
主
2° CO
OH2
intermediate
rearangemnt
product #1
(mincr)
3-Bromo-2-methylßentare.
or
3° CO
mere stable
intermediate
Br
product #2
(majar) blc
3° CO is mre.
Stalde than 2° CO
2-Bromo-2-methylpantane.
PRODUCTS!

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