ORGANIC CHEM PRINT STUDY GDE & SSM
ORGANIC CHEM PRINT STUDY GDE & SSM
4th Edition
ISBN: 9781119810650
Author: Klein
Publisher: WILEY
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Chapter 8.11, Problem 7LTS

(a)

Interpretation Introduction

Interpretation: The major product of the following reaction is to be interpreted.

  ORGANIC CHEM PRINT STUDY GDE & SSM, Chapter 8.11, Problem 7LTS , additional homework tip  1

Concept introduction:

The dihydroxylation reaction of alkene involves the addition of -OH group on the double-bonded carbon atom. It forms alkene to epoxide which further converts to trans-diol by the ring-opening reaction. The addition can occur in syn or anti-pattern that depends on the reagent.

(b)

Interpretation Introduction

Interpretation: The major product of the following reaction is to be interpreted.

  ORGANIC CHEM PRINT STUDY GDE & SSM, Chapter 8.11, Problem 7LTS , additional homework tip  2

Concept introduction:

The dihydroxylation reaction of alkene involves the addition of -OH group on the double-bonded carbon atom. It forms alkene to epoxide which further converts to trans-diol by the ring-opening reaction. The addition can occur in syn or anti-pattern that depends on the reagent.

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achieve.macmillanlearning.com Canvas EA eac h Hulu YouTube G 3 methyl cyclobutanol - Google Search Ranking Phenol Acidity Course -236 - Organic Chemistry - Mac... ← Assessment Completed 10 of 22 Questions 1 + Netflix paramount plus chem hw Galdehyde reaction with grignard reagent... b My Questions | bartleby M Inbox - chenteislegit@gmail.com - Gmail Due: Fri, Jan 31 Resources Solution Penalized ? Hint Submit Answer Use retrosynthetic analysis to suggest two paths to synthesize 2-methyl-3-hexanol using the Grignard reaction. (Click and drag the appropriate image to the correct position in the reactions.) Route 1 Aldehyde 1 or +98 Aldehyde 2 Route 2 Q6 +100 Solved in 1 attempt Q7 +95 Solved in 2 attempts Q8 +98 Unlimited attempts possible + + Grignard 1 OH H3O+ Grignard 2 Answer Bank Q9 +90 MgBr Unlimited attempts possible CH3CH2CH2MgBr Q10 Unlimited attempts Q11 ? ? +100 in 1 attempt 2-methyl-3-hexanol CH3CH2MgBr H H о H Attempt 3
2) (4 pt) After the reaction was completed, the student collected the following data. Crude product data is the data collected after the reaction is finished, but before the product is purified. "Pure" product data is the data collected after attempted purification using recrystallization. Student B's data: Crude product data "Pure" product data after recrystallization Crude mass: 0.93 g grey solid Crude mp: 96-106 °C Crude % yield: Pure mass: 0.39 g white solid Pure mp: 111-113 °C Pure % yield: a) Calculate the crude and pure percent yields for the student's reaction. b) Summarize what is indicated by the crude and pure melting points.
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