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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Transcribed Image Text:**Question:**
What is(are) the major product(s) of the following reaction?
**Reaction:**
- **Starting Material:** The compound consists of a carbon chain with an iodine (I) atom and a phenyl group (Ph). The iodine is attached to a chiral center.
- **Reagent:** CH₃OH is used in the reaction.
**Options:**
1. **Option A:**
- Structure: The original carbon chain with the methoxy group (OCH₃) replacing the iodine, and the configuration at the chiral center is retained (same orientation as starting material).
2. **Option B:**
- Structure: The original carbon chain with the methoxy group (OCH₃) replacing the iodine, but the configuration at the chiral center is inverted (opposite orientation to starting material).
3. **Option C:**
- Structure: The original carbon chain without any substitution at the originally iodinated chiral center, leaving only the phenyl group attached.
Each structure has a circle next to it, indicating a multiple-choice answer format.

Transcribed Image Text:The image contains a multiple-choice question with graphical representations of organic molecules depicted as follows:
1. **Option 1**: Structure showing a linear carbon chain with a methoxy group (OCH₃) and a phenyl group (Ph) attached.
2. **Option 2**: Structure showing a carbon chain with a double bond, terminating with a phenyl group (Ph).
3. **Option 3**: Structure showing a carbon chain with a triple bond, terminating with a phenyl group (Ph).
Below these options are multiple-choice answers:
- Two of the above (with a selection mark indicating this answer is chosen)
- Three of the above
- All of the above
This diagram is likely used to test knowledge of organic chemistry structures, emphasizing functional groups and bonding types.
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