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State the chemical formula for each compound.

Chemistry

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  1. State the chemical formula for each compound.

    • a) Nitrogen gas: Nitrogen exists as a diatomic molecule. N2\boxed{\text{N}_2}
    • b) Carbon (IV) oxide: Carbon with an oxidation state of +4, bonded to oxygen. This is commonly known as carbon dioxide. CO2\boxed{\text{CO}_2}
    • c) Ammonia: A common inorganic compound of nitrogen and hydrogen. NH3\boxed{\text{NH}_3}
  2. Name the following organic compounds.

    • i) CH3C(=O)OCH2CH3\text{CH}_3\text{C}(=\text{O})\text{OCH}_2\text{CH}_3 This is an ester. The acid part is derived from ethanoic acid (2 carbons), and the alcohol part is derived from ethanol (2 carbons). Ethyl ethanoate\boxed{\text{Ethyl ethanoate}}
    • ii) CH3CH2C(=O)OCH2CH2CH3\text{CH}_3\text{CH}_2\text{C}(=\text{O})\text{OCH}_2\text{CH}_2\text{CH}_3 This is an ester. The acid part is derived from propanoic acid (3 carbons), and the alcohol part is derived from propanol (3 carbons). Propyl propanoate\boxed{\text{Propyl propanoate}}
    • iii) CH3CH2CH2CH2OH\text{CH}_3\text{CH}_2\text{CH}_2\text{CH}_2\text{OH} This is a primary alcohol with a 4-carbon chain and the hydroxyl group on the first carbon. Butan-1-ol\boxed{\text{Butan-1-ol}}
  3. Draw the structural isomers of C5H10\text{C}_5\text{H}_{10}.

    The formula C5H10\text{C}_5\text{H}_{10} indicates that the compounds are either alkenes (containing one double bond) or cycloalkanes.

    • Alkenes:

      1. Pent-1-ene CH2=CH−CH2−CH2−CH3\text{CH}_2=\text{CH}-\text{CH}_2-\text{CH}_2-\text{CH}_3
      2. Pent-2-ene (cis and trans isomers exist, but only the structural isomer is shown) CH3−CH=CH−CH2−CH3\text{CH}_3-\text{CH}=\text{CH}-\text{CH}_2-\text{CH}_3
      3. 2-Methylbut-1-ene CH2=C(CH3)−CH2−CH3\text{CH}_2=\text{C}(\text{CH}_3)-\text{CH}_2-\text{CH}_3
      4. 3-Methylbut-1-ene CH2=CH−CH(CH3)−CH3\text{CH}_2=\text{CH}-\text{CH}(\text{CH}_3)-\text{CH}_3
      5. 2-Methylbut-2-ene CH3−C(CH3)=CH−CH3\text{CH}_3-\text{C}(\text{CH}_3)=\text{CH}-\text{CH}_3
    • Cycloalkanes: 6. Cyclopentane CH2−CH2∣∣CH2CH2\/CH2 \begin{smallmatrix} \text{CH}_2-\text{CH}_2 \\ | \quad \quad | \\ \text{CH}_2 \quad \text{CH}_2 \\ \quad \backslash / \\ \quad \text{CH}_2 \end{smallmatrix} 7. Methylcyclobutane CH(CH3)−CH2∣∣CH2CH2 \begin{smallmatrix} \text{CH}(\text{CH}_3)-\text{CH}_2 \\ | \quad \quad \quad | \\ \text{CH}_2 \quad \quad \text{CH}_2 \end{smallmatrix} 8. 1,1-Dimethylcyclopropane CH2/\C(CH3)2−CH2 \begin{smallmatrix} \quad \text{CH}_2 \\ \quad / \quad \backslash \\ \text{C}(\text{CH}_3)_2-\text{CH}_2 \end{smallmatrix} 9. 1,2-Dimethylcyclopropane (cis and trans isomers exist, but only the structural isomer is shown) CH(CH3)/\CH(CH3)−CH2 \begin{smallmatrix} \quad \text{CH}(\text{CH}_3) \\ \quad / \quad \quad \backslash \\ \text{CH}(\text{CH}_3)-\text{CH}_2 \end{smallmatrix} 10. Ethylcyclopropane CH2/\CH(CH2CH3)−CH2 \begin{smallmatrix} \quad \text{CH}_2 \\ \quad / \quad \backslash \\ \text{CH}(\text{CH}_2\text{CH}_3)-\text{CH}_2 \end{smallmatrix}

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