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C=O Bond Stretch

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Organic Chemistry

Definition

The C=O bond stretch refers to the vibrational mode of the carbon-oxygen double bond, which is a key structural feature in various organic compounds such as carboxylic acids and nitriles. This stretching vibration occurs when the carbon and oxygen atoms move closer and farther apart along the bond axis, causing changes in the bond length.

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5 Must Know Facts For Your Next Test

  1. The C=O bond stretch typically appears in the range of 1650-1850 cm$^{-1}$ in the infrared spectrum, making it a distinctive and easily identifiable feature.
  2. The exact position of the C=O bond stretch within this range can provide information about the specific type of carbonyl-containing compound, such as carboxylic acids or nitriles.
  3. The intensity and shape of the C=O bond stretch absorption band can be influenced by factors like hydrogen bonding, conjugation, and the environment surrounding the carbonyl group.
  4. Carboxylic acids exhibit a characteristic C=O bond stretch around 1700-1725 cm$^{-1}$, while nitriles show a sharper and more intense C=O bond stretch around 2220-2260 cm$^{-1}$.
  5. The C=O bond stretch is a valuable tool in organic structure elucidation, as it helps identify the presence and environment of carbonyl-containing functional groups in unknown compounds.

Review Questions

  • Explain how the position of the C=O bond stretch in the infrared spectrum can be used to differentiate between carboxylic acids and nitriles.
    • The C=O bond stretch in carboxylic acids typically appears around 1700-1725 cm$^{-1}$, while in nitriles, it appears at a higher wavenumber range of 2220-2260 cm$^{-1}$. This difference in the position of the C=O bond stretch is due to the different electronic environments and bonding patterns in these two functional groups. In carboxylic acids, the carbonyl group is conjugated with the hydroxyl group, which lowers the C=O bond stretch frequency. In contrast, the nitrile group has a more polarized C=N bond, leading to a higher C=O bond stretch frequency.
  • Describe how factors like hydrogen bonding and conjugation can influence the intensity and shape of the C=O bond stretch absorption band in the infrared spectrum.
    • The intensity and shape of the C=O bond stretch absorption band can be affected by various factors. Hydrogen bonding, where the carbonyl oxygen acts as a hydrogen bond acceptor, can lead to a broadening and shifting of the C=O bond stretch to lower wavenumbers. This is because hydrogen bonding weakens the C=O bond, reducing its vibrational frequency. Conjugation, where the carbonyl group is part of a larger π-system, can also influence the C=O bond stretch. Conjugation can cause a shift of the C=O bond stretch to lower wavenumbers and an increase in the intensity of the absorption band due to the delocalization of the π-electrons.
  • Analyze the importance of the C=O bond stretch in the structural elucidation of unknown organic compounds, particularly in the context of carboxylic acids and nitriles.
    • The C=O bond stretch is a crucial tool in the structural elucidation of unknown organic compounds, especially in the identification of carbonyl-containing functional groups like carboxylic acids and nitriles. The distinctive position of the C=O bond stretch in the infrared spectrum, along with its intensity and shape, can provide valuable information about the type of carbonyl group present. For example, the C=O bond stretch around 1700-1725 cm$^{-1}$ indicates the presence of a carboxylic acid, while the sharper and more intense C=O bond stretch around 2220-2260 cm$^{-1}$ suggests the presence of a nitrile group. This information, combined with other spectroscopic data and chemical reactivity, can be used to elucidate the overall structure of unknown organic compounds, which is essential in fields such as organic synthesis, natural product isolation, and pharmaceutical development.

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