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  2. Mesomeric effect - Wikipedia

    en.wikipedia.org/wiki/Mesomeric_effect

    In chemistry, the mesomeric effect (or resonance effect) is a property of substituents or functional groups in a chemical compound. It is defined as the polarity produced in the molecule by the interaction of two pi bonds or between a pi bond and lone pair of electrons present on an adjacent atom. [ 1 ]

  3. Resonance (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Resonance_(chemistry)

    Contributing structures of the carbonate ion. In chemistry, resonance, also called mesomerism, is a way of describing bonding in certain molecules or polyatomic ions by the combination of several contributing structures (or forms, [1] also variously known as resonance structures or canonical structures) into a resonance hybrid (or hybrid structure) in valence bond theory.

  4. Nitrobenzene - Wikipedia

    en.wikipedia.org/wiki/Nitrobenzene

    Nitrobenzene is an aromatic nitro compound and the simplest of the nitrobenzenes, with the chemical formula C 6 H 5 NO 2. It is a water-insoluble pale yellow oil with an almond -like odor. It freezes to give greenish-yellow crystals.

  5. Category:Nitrobenzenes - Wikipedia

    en.wikipedia.org/wiki/Category:Nitrobenzenes

    If the benzene ring contains other substituents, it belongs in Category:Nitrobenzene derivatives Wikimedia Commons has media related to Nitrobenzenes . The main article for this category is Nitrobenzenes .

  6. Benzidine - Wikipedia

    en.wikipedia.org/wiki/Benzidine

    Benzidine is prepared in a two step process from nitrobenzene. First, the nitrobenzene is converted to 1,2-diphenylhydrazine , usually using iron powder as the reducing agent. Treatment of this hydrazine with mineral acids induces a rearrangement reaction to 4,4'-benzidine.

  7. Resonance Raman spectroscopy - Wikipedia

    en.wikipedia.org/wiki/Resonance_Raman_spectroscopy

    Typically, resonance Raman spectroscopy is performed in the same manner as ordinary Raman spectroscopy, using a single laser light source to excite the sample. The difference is the choice of the laser wavelength, which must be selected to match the energy of an electronic transition in the sample.

  8. Talk:Resonance (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Talk:Resonance_(chemistry)

    The term resonance hybrid would be meaningless. Or would the resonance hybrid be the structure with the lowest possible energy? That would implicate that the resonance hybrid is the structure that reflects the real compound. --Wickey-nl 10:51, 5 May 2010 (UTC) "Weighted average" is not totally correct here.

  9. 4-Nitrobenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/4-Nitrobenzaldehyde

    4-Nitrobenzaldehyde is an organic compound with the formula O 2 NC 6 H 4 CHO.It is one of three isomers of nitrobenzaldehyde. It contains a nitro group para-substituted to an aldehyde.