a)
Interpretation:
What is wrong with the synthetic route given is to be stated.
Concept introduction:
To state:
What is wrong with the synthetic route given?
b)
Interpretation:
What is wrong with the synthetic route given is to be stated.
Concept introduction:
Acetoacetic ester when treated with sodium ethoxide yields an enolate anion. The enolate ion will undergo a SN2 displacement reaction with primary
To state:
What is wrong with the synthetic route given?
c)
Interpretation:
What is wrong with the synthetic route given is to be stated.
Concept introduction:
Acetoacetic ester synthesis can be used to prepare methyl ketones. Carboxylic acids can be prepared by malonic ester synthesis.
To state:
What is wrong with the synthetic route shown?
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Chapter 22 Solutions
ORGANIC CHEMISTRY-EBOOK>I<
- Consider the following reaction sequence. Identify the missing reagents.arrow_forwardSynthesize the product from the given material. Give the reagents necessary and draw out any intermediate products along the way.arrow_forwardChoose the best reagents to complete the following reaction.arrow_forward
- Match each reagent to the product that it forms. Multiple reagents may form the same product. HO Reagent Reagents SOCI2, pyridine: C CISO2CH3, pyridine: E HCI: A PCI 3: A A) B) "It eft ft D) E) F) "got soft soft MSO MsO CIarrow_forwardDraw the synthons and synthetic equivalents for the following compounds. a) c) Meo b) d) O,N `NO2arrow_forward4. WHAT ARE IMINES? HOW ARE THEY FORMED? 5. WHAT IS GRIGNARD REACTION? WHAT CONSTITUTES A GRIGNARD REAGENT? 6. WHAT IS KETO-ENOL TAUTOMERIZATION?arrow_forward
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