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  2. Carbonyl group - Wikipedia

    en.wikipedia.org/wiki/Carbonyl_group

    The polarity of C=O bond also enhances the acidity of any adjacent C-H bonds. Due to the positive charge on carbon and the negative charge on oxygen, carbonyl groups are subject to additions and/or nucleophilic attacks. A variety of nucleophiles attack, breaking the carbon-oxygen double bond, and leading to addition-elimination reactions.

  3. Carbon–oxygen bond - Wikipedia

    en.wikipedia.org/wiki/Carbonoxygen_bond

    A carbon–oxygen bond is a polar covalent bond between atoms of carbon and oxygen. [1] [2] [3]: 16–22 Carbon–oxygen bonds are found in many inorganic compounds such as carbon oxides and oxohalides, carbonates and metal carbonyls, [4] and in organic compounds such as alcohols, ethers, and carbonyl compounds.

  4. Double bond - Wikipedia

    en.wikipedia.org/wiki/Double_bond

    Double bonds occur most commonly between two carbon atoms, for example in alkenes. Many double bonds exist between two different elements: for example, in a carbonyl group between a carbon atom and an oxygen atom. Other common double bonds are found in azo compounds (N=N), imines (C=N), and sulfoxides (S=O). In a skeletal formula, a double bond ...

  5. Carbon dioxide - Wikipedia

    en.wikipedia.org/wiki/Carbon_dioxide

    Carbon dioxide is a chemical compound with the chemical formula CO 2.It is made up of molecules that each have one carbon atom covalently double bonded to two oxygen atoms. It is found in the gas state at room temperature and at normally-encountered concentrations it is odorless.

  6. Double bond rule - Wikipedia

    en.wikipedia.org/wiki/Double_bond_rule

    Double bonds for carbon and nearest neighbours B boron (n=2) C carbon (n=2) N ... Singlet oxygen: silanones, Si=O bonds extremely reactive, oligomerization to siloxanes:

  7. Formal charge - Wikipedia

    en.wikipedia.org/wiki/Formal_charge

    Carbon double bonded to both oxygen atoms (carbon = 0, oxygens = 0, total formal charge = 0) Even though all three structures gave us a total charge of zero, the final structure is the superior one because there are no charges in the molecule at all.

  8. Oxocarbenium - Wikipedia

    en.wikipedia.org/wiki/Oxocarbenium

    The best Lewis structure for an oxocarbenium ion contains an oxygen–carbon double bond, with the oxygen atom attached to an additional group and consequently taking on a formal positive charge. In the language of canonical structures (or "resonance"), the polarization of the π bond is described by a secondary carbocationic resonance form ...

  9. Aldehyde - Wikipedia

    en.wikipedia.org/wiki/Aldehyde

    Aldehyde molecules have a central carbon atom that is connected by a double bond to oxygen, a single bond to hydrogen and another single bond to a third substituent, which is carbon or, in the case of formaldehyde, hydrogen. The central carbon is often described as being sp 2-hybridized. The aldehyde group is somewhat polar.