Which of the following reaction is a correct procedure to prepare alkenes. a. b. C. a C Br OH Br a OH KOH CH3CH₂OH H₂SO4, H₂O THF, 50 °C H₂SO4, H₂O THF, 50 °C KOH CH3CH₂OH Br Br
Which of the following reaction is a correct procedure to prepare alkenes. a. b. C. a C Br OH Br a OH KOH CH3CH₂OH H₂SO4, H₂O THF, 50 °C H₂SO4, H₂O THF, 50 °C KOH CH3CH₂OH Br Br
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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![**Question 4**
Which of the following reactions is a correct procedure to prepare alkenes?
**a.**
A cyclohexane ring with a bromine (Br) substituent reacts with KOH in ethanol (CH₃CH₂OH). The product is a cyclohexene ring with a double bond.
**b.**
A cyclohexanol (cyclohexane ring with an OH group) reacts with H₂SO₄ and H₂O in THF at 50°C. The product is a cyclohexene ring with a double bond.
**c.**
A cyclohexane ring with a bromine (Br) substituent reacts with H₂SO₄ and H₂O in THF at 50°C. The product is a cyclohexene ring with a double bond.
**d.**
A cyclohexanol reacts with KOH in ethanol (CH₃CH₂OH). The product is a cyclohexene ring with a double bond.
- [ ] a
- [ ] b
- [ ] c
- [ ] d
**Question 5**
What is the major product of the following reaction? (Details not provided in the image)](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Ff4bad56a-42cf-4354-a699-f947a893672e%2F39955529-e555-45a5-adfb-f7729b6327c3%2Fzmxd608_processed.jpeg&w=3840&q=75)
Transcribed Image Text:**Question 4**
Which of the following reactions is a correct procedure to prepare alkenes?
**a.**
A cyclohexane ring with a bromine (Br) substituent reacts with KOH in ethanol (CH₃CH₂OH). The product is a cyclohexene ring with a double bond.
**b.**
A cyclohexanol (cyclohexane ring with an OH group) reacts with H₂SO₄ and H₂O in THF at 50°C. The product is a cyclohexene ring with a double bond.
**c.**
A cyclohexane ring with a bromine (Br) substituent reacts with H₂SO₄ and H₂O in THF at 50°C. The product is a cyclohexene ring with a double bond.
**d.**
A cyclohexanol reacts with KOH in ethanol (CH₃CH₂OH). The product is a cyclohexene ring with a double bond.
- [ ] a
- [ ] b
- [ ] c
- [ ] d
**Question 5**
What is the major product of the following reaction? (Details not provided in the image)
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