4. a)Nucleophiles. Define a "nucleophile" in organic chemistry? b) Identifying nucleophiles. Bronsted-Lowry acid-base pairs are shown. Which one in each pair can serve as a nucleophile in an organic nucleohilic reaction. (Explain your choice.) It is helpful sometimes to draw in all the lone-pairs of electrons. Son lo H3O+ or H₂O or H-Br or Br OH

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**4. a) Nucleophiles. Define a "nucleophile" in organic chemistry.**

A nucleophile is a chemical species that donates an electron pair to an electrophile to form a chemical bond in relation to a reaction. In other words, nucleophiles are typically negatively charged or neutral species with lone pairs of electrons that are attracted to positively charged or electron-deficient sites on other molecules.

**b) Identifying nucleophiles. Bronsted-Lowry acid-base pairs are shown. Which one in each pair can serve as a nucleophile in an organic nucleophilic reaction? (Explain your choice.) It is helpful sometimes to draw in all the lone-pairs of electrons.**

- **H—Br** or **Br⁻**
- **Br⁻** can be a nucleophile because it has a lone pair of electrons that it can donate.

- **CH₃NH₂** or **CH₃NH₃⁺**
- **CH₃NH₂** can be a nucleophile because it has a lone pair of electrons on the nitrogen atom that it can donate.

- **⁻C≡N** or **HC≡N**
- **⁻C≡N** (cyanide ion, with a negative charge) can be a nucleophile because it has a lone pair of electrons that it can donate.

- **O═C═O** or **⁻O—C≡N**
- **⁻O—C≡N** can be a nucleophile because it has a lone pair of electrons on the oxygen atom that it can donate.

- **O═C═O** or **O--C≡N**
- **H₃O⁺** or **H₂O**
- **H₂O** can be a nucleophile because it has lone pairs of electrons that it can donate.
Transcribed Image Text:**4. a) Nucleophiles. Define a "nucleophile" in organic chemistry.** A nucleophile is a chemical species that donates an electron pair to an electrophile to form a chemical bond in relation to a reaction. In other words, nucleophiles are typically negatively charged or neutral species with lone pairs of electrons that are attracted to positively charged or electron-deficient sites on other molecules. **b) Identifying nucleophiles. Bronsted-Lowry acid-base pairs are shown. Which one in each pair can serve as a nucleophile in an organic nucleophilic reaction? (Explain your choice.) It is helpful sometimes to draw in all the lone-pairs of electrons.** - **H—Br** or **Br⁻** - **Br⁻** can be a nucleophile because it has a lone pair of electrons that it can donate. - **CH₃NH₂** or **CH₃NH₃⁺** - **CH₃NH₂** can be a nucleophile because it has a lone pair of electrons on the nitrogen atom that it can donate. - **⁻C≡N** or **HC≡N** - **⁻C≡N** (cyanide ion, with a negative charge) can be a nucleophile because it has a lone pair of electrons that it can donate. - **O═C═O** or **⁻O—C≡N** - **⁻O—C≡N** can be a nucleophile because it has a lone pair of electrons on the oxygen atom that it can donate. - **O═C═O** or **O--C≡N** - **H₃O⁺** or **H₂O** - **H₂O** can be a nucleophile because it has lone pairs of electrons that it can donate.
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