How could you obtain the two products shown below from 1-bromo-1-methylcyclohexane (just write the order of reagent used)?

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
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**Question:**

How could you obtain the two products shown below from 1-bromo-1-methylcyclohexane (just write the order of reagent used)?

**Diagram:**

The diagram shows two chemical structures:

1. The first structure is cyclohexanone, which is a six-membered carbon ring with a ketone group (C=O) attached.

2. The second structure is formaldehyde, which is the simplest aldehyde with the formula H2CO, consisting of a carbonyl group (C=O) bonded to two hydrogen atoms. 

**Note:** The question asks for the sequence of reagents needed to transform 1-bromo-1-methylcyclohexane into these two products.
Transcribed Image Text:**Question:** How could you obtain the two products shown below from 1-bromo-1-methylcyclohexane (just write the order of reagent used)? **Diagram:** The diagram shows two chemical structures: 1. The first structure is cyclohexanone, which is a six-membered carbon ring with a ketone group (C=O) attached. 2. The second structure is formaldehyde, which is the simplest aldehyde with the formula H2CO, consisting of a carbonyl group (C=O) bonded to two hydrogen atoms. **Note:** The question asks for the sequence of reagents needed to transform 1-bromo-1-methylcyclohexane into these two products.
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