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  2. Nucleophile - Wikipedia

    en.wikipedia.org/wiki/Nucleophile

    A hydroxide ion acting as a nucleophile in an S N 2 reaction, converting a haloalkane into an alcohol. In chemistry, a nucleophile is a chemical species that forms bonds by donating an electron pair. All molecules and ions with a free pair of electrons or at least one pi bond can act as nucleophiles. Because nucleophiles donate electrons, they ...

  3. RNA hydrolysis - Wikipedia

    en.wikipedia.org/wiki/RNA_hydrolysis

    RNA hydrolysis occurs when the deprotonated 2’ OH of the ribose, acting as a nucleophile, attacks the adjacent phosphorus in the phosphodiester bond of the sugar-phosphate backbone of the RNA. [1] There is a transition state (shown above), where the phosphorus is bonded to five oxygen atoms. [ 2 ]

  4. Non-nucleophilic base - Wikipedia

    en.wikipedia.org/wiki/Non-nucleophilic_base

    As the name suggests, a non-nucleophilic base is a sterically hindered organic base that is a poor nucleophile.Normal bases are also nucleophiles, but often chemists seek the proton-removing ability of a base without any other functions.

  5. Ambident (chemistry) - Wikipedia

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

    An Ambident nucleophile refers to an anionic nucleophile that exhibits resonance delocalization of its negative charge over two unlike atoms or over two like but non-equivalent atoms. Enolate ions are Ambident Nucleophile.

  6. 2,4-Dinitrophenylhydrazine - Wikipedia

    en.wikipedia.org/wiki/2,4-Dinitrophenylhydrazine

    2,4-Dinitrophenylhydrazine (2,4-DNPH or DNPH) is the organic compound C 6 H 3 (NO 2) 2 NHNH 2. DNPH is a red to orange solid. It is a substituted hydrazine. The solid is relatively sensitive to shock and friction. For this reason DNPH is usually handled as a wet powder. DNPH is a precursor to the drug Sivifene.

  7. Lithium diisopropylamide - Wikipedia

    en.wikipedia.org/wiki/Lithium_diisopropylamide

    Lithium diisopropylamide (commonly abbreviated LDA) is a chemical compound with the molecular formula LiN(CH(CH 3) 2) 2. It is used as a strong base and has been widely utilized due to its good solubility in non-polar organic solvents and non-nucleophilic nature. It is a colorless solid, but is usually generated and observed only in solution.

  8. List of RNAs - Wikipedia

    en.wikipedia.org/wiki/List_of_RNAs

    Function Distribution Ref. Antisense RNA: aRNA, asRNA: Transcriptional attenuation / mRNA degradation / mRNA stabilisation / Translation block: All organisms [11] [12] Cis-natural antisense transcript: cis-NAT Gene regulation: CRISPR RNA: crRNA: Resistance to parasites, by targeting their DNA: Bacteria and archaea [13] Long noncoding RNA: lncRNA

  9. Williamson ether synthesis - Wikipedia

    en.wikipedia.org/wiki/Williamson_ether_synthesis

    In order for the S N 2 reaction to take place there must be a good leaving group which is strongly electronegative, commonly a halide. [4] In the Williamson ether reaction there is an alkoxide ion (RO −) which acts as the nucleophile, attacking the electrophilic carbon with the leaving group, which in most cases is an alkyl tosylate or an ...