20:24 1 : 10. Draw the full cleavage of 2-ethoxypropane by HCI scheme on your paper, and then draw in the curved arrows for each step of the mechanism. HICI co OⓇ ← H₂O 11. What reagent can be used to convert 2-methylbutan-1-ol into 2-methylbutanal? A) Bleach B) LIAIH4 C) DMSO, (COCI)2, TEA D) Na₂Cr₂O7, H₂SO4 E) 03 12. Fill in the box with the major organic product of the first step of the reaction shown? H-Cl Send a chat O

20:24 1 : 10. Draw the full cleavage of 2-ethoxypropane by HCI scheme on your paper, and then draw in the curved arrows for each step of the mechanism. HICI co OⓇ ← H₂O 11. What reagent can be used to convert 2-methylbutan-1-ol into 2-methylbutanal? A) Bleach B) LIAIH4 C) DMSO, (COCI)2, TEA D) Na₂Cr₂O7, H₂SO4 E) 03 12. Fill in the box with the major organic product of the first step of the reaction shown? H-Cl Send a chat O

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

Chapter21: Benzene And The Concept Of Aromaticity

Section: Chapter Questions

Problem 21.58P

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20:25 : E) Grignard 16. Acid chlorides can be prepared from carboxylic acids by treatment with A) KCI B) (COCI)2 C) SOCI₂ D) both (COCI)2 and SOCI₂ E) both SOCI₂ and KCI 17. Provide the major organic product of the reaction shown. Find your most reactive electrons. Where will they go? Check to see if the intermediate has a good leaving group. If so, check to see if you have enough of the nucleophile to repeat nucleophilic attack. 1. Me-MgBr (xs) 2. H₂O+ Send a chat O
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