Predict the major product(s) of the following reactions. Justify your reasoning for the product you chose in a sentence. You may assume each step is followed by an aqueous workup that neutralizes any leftover reagents and/or charge on the compound.

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Predict the major product(s) of the following reactions. Justify your reasoning for the product you chose in a sentence. You may assume each step is followed by an aqueous workup that neutralizes any leftover reagents and/or charge on the compound.

The image shows two chemical reactions involving organic compounds. Each reaction is depicted with starting materials, reagents, and conditions.

1. **Reaction One:**
   - **Starting Material:** An organic compound with an ester functional group and a conjugated double bond.
   - **Reagent:** Sodium azide (NaN₃).
   - **Condition:** The reaction is carried out at 100°C.
   - There is an arrow indicating that the reaction leads to a new product, although the specific product is not shown in this image.

2. **Reaction Two:**
   - **Starting Material:** An organic compound with a brominated ketone.
   - **Reagent:** Sodium ethoxide (NaOEt).
   - **Condition:** The reaction is conducted in ethanol (EtOH) at 4°C.
   - An arrow indicates the progression to the product, which is not explicitly shown in the image.

These reactions are typical in organic synthesis, involving nucleophilic substitutions or other transformations under specified conditions.
Transcribed Image Text:The image shows two chemical reactions involving organic compounds. Each reaction is depicted with starting materials, reagents, and conditions. 1. **Reaction One:** - **Starting Material:** An organic compound with an ester functional group and a conjugated double bond. - **Reagent:** Sodium azide (NaN₃). - **Condition:** The reaction is carried out at 100°C. - There is an arrow indicating that the reaction leads to a new product, although the specific product is not shown in this image. 2. **Reaction Two:** - **Starting Material:** An organic compound with a brominated ketone. - **Reagent:** Sodium ethoxide (NaOEt). - **Condition:** The reaction is conducted in ethanol (EtOH) at 4°C. - An arrow indicates the progression to the product, which is not explicitly shown in the image. These reactions are typical in organic synthesis, involving nucleophilic substitutions or other transformations under specified conditions.
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