please help me answer all even without explanation 2. Draw the product of the propanol with HBr. Show the mechanism.3. Show how a 1,2-shift forms a more stable carbocation form each intermediate.a. (CHa),CHCHCH,CH3C.b.4. Draw the product/s of the reaction, indicating the stereochemistry around any stereogeniccenters.HỌ CH3HCI5. What product/s would you expect from dehydration of the following alcohols with POClzinpyridine? Indicate the major product in each case.(a)он(b)HCH3CH2CHCHCH3HOČH3CH3H.

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Answered: mechanism.

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mechanism.

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter13: Substitution

Section: Chapter Questions

Problem 13E

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Concept explainers

Designing a Synthesis

Organic synthesis is a branch of chemical synthesis that involves the planned construction of organic compounds/molecules from smaller units that possess functional groups. Friedrich Wöhler was the first scientist who designed the synthesis of an organic compound, urea from inorganic starting materials silver cyanate with ammonium chloride via a simple, one-step synthesis.

Question

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please help me answer all even without explanation

2. Draw the product of the propanol with HBr. Show the mechanism.
3. Show how a 1,2-shift forms a more stable carbocation form each intermediate.
a. (CHa),CHCHCH,CH3
C.
b.
4. Draw the product/s of the reaction, indicating the stereochemistry around any stereogenic
centers.
HỌ CH3
HCI
5. What product/s would you expect from dehydration of the following alcohols with POClzin
pyridine? Indicate the major product in each case.
(a)
он
(b)
H
CH3CH2CHCHCH3
HO
ČH3
CH3
H.

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