When.com Web Search

Search results

  1. Results From The WOW.Com Content Network
  2. Infrared spectroscopy correlation table - Wikipedia

    en.wikipedia.org/wiki/Infrared_spectroscopy...

    aldehyde/ketone saturated aliph./cyclic 6-membered 1720 α,β-unsaturated 1685 aromatic ketones 1685 cyclic 5-membered 1750 cyclic 4-membered 1775 aldehydes 1725 influenced by conjugation (as with ketones) carboxylic acids/derivates saturated carboxylic acids 1710 unsat./aromatic carb. acids 1680–1690 esters and lactones: 1735

  3. Mass spectral interpretation - Wikipedia

    en.wikipedia.org/wiki/Mass_spectral_interpretation

    There are five types of carbonyl compounds, including aldehydes, ketones, carboxylic acids and esters. [2] The principal fragmentation modes are described as follows: Alpha-cleavage can occur on either side of the carbonyl functional group since an oxygen lone pair can stabilize the positive charge. Alpha cleavage of carbonyl compounds

  4. Fehling's solution - Wikipedia

    en.wikipedia.org/wiki/Fehling's_solution

    In organic chemistry, Fehling's solution is a chemical reagent used to differentiate between water-soluble carbohydrate and ketone (>C=O) functional groups, and as a test for reducing sugars and non-reducing sugars, supplementary to the Tollens' reagent test. The test was developed by German chemist Hermann von Fehling in 1849. [1]

  5. Aldehyde - Wikipedia

    en.wikipedia.org/wiki/Aldehyde

    Aldehyde structure. In organic chemistry, an aldehyde (/ ˈ æ l d ɪ h aɪ d /) is an organic compound containing a functional group with the structure R−CH=O. [1] The functional group itself (without the "R" side chain) can be referred to as an aldehyde but can also be classified as a formyl group. Aldehydes are a common motif in many ...

  6. Oxime - Wikipedia

    en.wikipedia.org/wiki/Oxime

    The condensation of aldehydes with hydroxylamine gives aldoximes, and ketoximes are produced from ketones and hydroxylamine. In general, oximes exist as colorless crystals or as thick liquids and are poorly soluble in water. Therefore, oxime formation can be used for the identification of ketone or aldehyde functional groups.

  7. Fragmentation (mass spectrometry) - Wikipedia

    en.wikipedia.org/wiki/Fragmentation_(mass...

    Sigma bond cleavage also occurs on radical cations remote from the site of ionization. This is commonly observed in alcohols, ethers, ketones, esters, amines, alkenes, and aromatic compounds with a carbon attached to ring. The cation has a radical on a heteroatom or an unsaturated functional group. The driving force of fragmentation is the ...

  8. Functional group - Wikipedia

    en.wikipedia.org/wiki/Functional_group

    The reactivity of a functional group can be modified by other functional groups nearby. Functional group interconversion can be used in retrosynthetic analysis to plan organic synthesis. A functional group is a group of atoms in a molecule with distinctive chemical properties, regardless of the other atoms in the molecule. The atoms in a ...

  9. Transition metal complexes of aldehydes and ketones

    en.wikipedia.org/wiki/Transition_metal_complexes...

    In monometallic complexes, aldehydes and ketones can bind to metals in either of two modes, η 1-O-bonded and η 2-C,O-bonded. These bonding modes are sometimes referred to sigma- and pi-bonded. These forms may sometimes interconvert. The sigma bonding mode is more common for higher valence, Lewis-acidic metal centers (e.g., Zn 2+). [1]