for both pics, can you please see what the arrow notation is in the structure for the reaction mechanism. Please draw it clear and direct so I can understand. ОНH,SO4H3C-CH-CH2-CH3H3C-CH=CH-CH3H20cid-catalyzed dehydration of 2-butanol yields 2-butene as the major product. Draw curved arrows to show the movement oflectrons in this step of the reaction mechanism.Arrow-pushing InstructionsH-ÖHH3C-CH-CH2-CH3 H-O*-HH3C-CH-CH2-CH3H-ö- CIHCIH3CCH3H2C`CH3H;CCH3CIH2C`CH3H2C`CH3ČITreating 1,3-pentadiene with one mole of HCl give a mixture of five isomeric products. Draw curved arrows to show the movementof electrons in this step of the reaction mechanism.Arrow-pushing InstructionsCH3`CH2`CH3

Answered: Image /qna-images/answer/13cee327-138b-4ebe-9490-dc5d2ba01bda.jpg

Answered: for both pics, can you please see what…

for both pics, can you please see what the arrow notation is in the structure for the reaction mechanism. Please draw it clear and direct so I can understand.

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter20: Dienes, Conjugated Systems, And Pericyclic Reactions

Section: Chapter Questions

Problem 20.42P: Bicyclo-2,5-heptadiene can be prepared in two steps from cyclopentadiene and vinyl chloride. Provide...

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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.

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for both pics, can you please see what the arrow notation is in the structure for the reaction mechanism. Please draw it clear and direct so I can understand.

ОН
H,SO4
H3C-CH-CH2-CH3
H3C-CH=CH-CH3
H20
cid-catalyzed dehydration of 2-butanol yields 2-butene as the major product. Draw curved arrows to show the movement of
lectrons in this step of the reaction mechanism.
Arrow-pushing Instructions
H-ÖH
H3C-CH-CH2-CH3 H-O*-H
H3C-CH-CH2-CH3
H-ö-

CI
HCI
H3C
CH3
H2C
`CH3
H;C
CH3
CI
H2C
`CH3
H2C
`CH3
ČI
Treating 1,3-pentadiene with one mole of HCl give a mixture of five isomeric products. Draw curved arrows to show the movement
of electrons in this step of the reaction mechanism.
Arrow-pushing Instructions
CH3
`CH2
`CH3

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