Which set of conditions will give the product shown in this reaction? Br

Biochemistry
9th Edition
ISBN:9781319114671
Author:Lubert Stryer, Jeremy M. Berg, John L. Tymoczko, Gregory J. Gatto Jr.
Publisher:Lubert Stryer, Jeremy M. Berg, John L. Tymoczko, Gregory J. Gatto Jr.
Chapter1: Biochemistry: An Evolving Science
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**Transcription: Reaction Conditions for Elimination**

**Question:**  
Which set of conditions will give the product shown in this reaction?

**Reaction Diagram:**  
On the left side of the reaction arrow is a cyclohexane ring with a bromine (Br) substituent. The right side of the arrow shows a cyclohexene ring, indicating the presence of a double bond, illustrating an elimination reaction.

**Answer Options:**

1. KOH, ethanol and heat
2. Water/acetone and heat
3. tert-butoxide/tert-butyl alcohol
4. **tert-butyl alcohol and heat** (This option is selected)
5. Methoxide/methanol 

The reaction involves the elimination of bromine, resulting in the formation of a double bond on the cyclohexane ring. The conditions that best facilitate this transformation involve the use of tert-butyl alcohol and heat, as indicated by the selected option.
Transcribed Image Text:**Transcription: Reaction Conditions for Elimination** **Question:** Which set of conditions will give the product shown in this reaction? **Reaction Diagram:** On the left side of the reaction arrow is a cyclohexane ring with a bromine (Br) substituent. The right side of the arrow shows a cyclohexene ring, indicating the presence of a double bond, illustrating an elimination reaction. **Answer Options:** 1. KOH, ethanol and heat 2. Water/acetone and heat 3. tert-butoxide/tert-butyl alcohol 4. **tert-butyl alcohol and heat** (This option is selected) 5. Methoxide/methanol The reaction involves the elimination of bromine, resulting in the formation of a double bond on the cyclohexane ring. The conditions that best facilitate this transformation involve the use of tert-butyl alcohol and heat, as indicated by the selected option.
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