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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. Nitrogen dioxide - Wikipedia

    en.wikipedia.org/wiki/Nitrogen_dioxide

    Nitrogen dioxide is a chemical compound with the formula NO 2.One of several nitrogen oxides, nitrogen dioxide is a reddish-brown gas.It is a paramagnetic, bent molecule with C 2v point group symmetry.

  5. 1,3-dipole - Wikipedia

    en.wikipedia.org/wiki/1,3-dipole

    The dipole has at least one resonance structure with positive and negative charges having a 1,3 relationship which can generally be denoted as + a−b−c −, where a may be a carbon, oxygen or nitrogen, b may be nitrogen or oxygen, and c may be a carbon, oxygen or nitrogen. [3]

  6. Nitro compound - Wikipedia

    en.wikipedia.org/wiki/Nitro_compound

    Chloramphenicol is a rare example of a naturally occurring nitro compound. At least some naturally occurring nitro groups arose by the oxidation of amino groups. [17] 2-Nitrophenol is an aggregation pheromone of ticks. Examples of nitro compounds are rare in nature. 3-Nitropropionic acid found in fungi and plants .

  7. Lewis structure - Wikipedia

    en.wikipedia.org/wiki/Lewis_structure

    Expressing resonance when drawing Lewis structures may be done either by drawing each of the possible resonance forms and placing double-headed arrows between them or by using dashed lines to represent the partial bonds (although the latter is a good representation of the resonance hybrid which is not, formally speaking, a Lewis structure).

  8. NOx - Wikipedia

    en.wikipedia.org/wiki/NOx

    NO 2 also reacts with ozone to form nitrate radical NO 2 + O 3 → NO 3 + O 2. During the daytime, NO 3 is quickly photolyzed back to NO 2, but at night it can react with a second NO 2 to form dinitrogen pentoxide. NO 2 + NO 3 (+M) → N 2 O 5 (+M). N 2 O 5 reacts rapidly with liquid water (in aerosol particles or cloud drops, but not in the ...

  9. Diazo - Wikipedia

    en.wikipedia.org/wiki/Diazo

    Diazo compounds have two main Lewis structures in resonance: R 2 >C − –N + ≡N and R 2 >CH=N + =N −. In organic chemistry, the diazo group is an organic moiety consisting of two linked nitrogen atoms at the terminal position.