Provide the reaction mechanisms outlined in the two hand drawn examples below. + HgO Br CH3 CH3 + tBuOH 1h CHz H,C CH.

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**Provide the reaction mechanisms** outlined in the two hand-drawn examples below.

**Example 1:**
- The reaction involves a mechanism with a hydroxide ion (\[OH^-\]) and hydrobromic acid (\[HBr\]).
- The hydroxide ion attacks the hydrogen atom, forming water (\[H_2O\]).
- The bromide ion (\[Br^-\]) leaves, resulting in the formation of a new molecule, 2-butanol, along with water and bromide ions as products.

**Example 2:**
- The reaction involves the tert-butoxide ion (\[tBuO^-\]) and hydrogen bromide (\[HBr\]).
- The tert-butoxide ion abstracts a proton (\[H^+\]) from the starting compound, forming a double bond and resulting in an elimination reaction.
- The final product is an alkene (2-methylpropene) along with tert-butanol and a bromide ion as byproducts.

These examples illustrate classic organic reaction mechanisms involving nucleophilic substitution and elimination pathways.
Transcribed Image Text:**Provide the reaction mechanisms** outlined in the two hand-drawn examples below. **Example 1:** - The reaction involves a mechanism with a hydroxide ion (\[OH^-\]) and hydrobromic acid (\[HBr\]). - The hydroxide ion attacks the hydrogen atom, forming water (\[H_2O\]). - The bromide ion (\[Br^-\]) leaves, resulting in the formation of a new molecule, 2-butanol, along with water and bromide ions as products. **Example 2:** - The reaction involves the tert-butoxide ion (\[tBuO^-\]) and hydrogen bromide (\[HBr\]). - The tert-butoxide ion abstracts a proton (\[H^+\]) from the starting compound, forming a double bond and resulting in an elimination reaction. - The final product is an alkene (2-methylpropene) along with tert-butanol and a bromide ion as byproducts. These examples illustrate classic organic reaction mechanisms involving nucleophilic substitution and elimination pathways.
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