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  2. Tollens' reagent - Wikipedia

    en.wikipedia.org/wiki/Tollens'_reagent

    Tollens' test for aldehyde: left side positive (silver mirror), right side negative Ball-and-stick model of the diamminesilver(I) complex Tollens' reagent (chemical formula Ag ( NH 3 ) 2 OH {\displaystyle {\ce {Ag(NH3)2OH}}} ) is a chemical reagent used to distinguish between aldehydes and ketones along with some alpha-hydroxy ketones which can ...

  3. Zeisel determination - Wikipedia

    en.wikipedia.org/wiki/Zeisel_determination

    The Zeisel determination or Zeisel test is a chemical test for the presence of esters or ethers in a chemical substance. [1] [2] [3] [4]It is named after the Czech chemist Simon Zeisel (1854–1933).

  4. List of esters - Wikipedia

    en.wikipedia.org/wiki/List_of_esters

    An ester of carboxylic acid.R stands for any group (organic or inorganic) and R′ stands for organyl group.. In chemistry, an ester is a compound derived from an acid (organic or inorganic) in which the hydrogen atom (H) of at least one acidic hydroxyl group (−OH) of that acid is replaced by an organyl group (−R).

  5. Ester - Wikipedia

    en.wikipedia.org/wiki/Ester

    Esters of propanoic acid are produced commercially by this method: H 2 C=CH 2 + ROH + CO → CH 3 CH 2 CO 2 R. A preparation of methyl propionate is one illustrative example. H 2 C=CH 2 + CO + CH 3 OH → CH 3 CH 2 CO 2 CH 3. The carbonylation of methanol yields methyl formate, which is the main commercial source of formic acid. The reaction is ...

  6. Acetyl chloride - Wikipedia

    en.wikipedia.org/wiki/Acetyl_chloride

    Acetyl chloride is a reagent for the preparation of esters and amides of acetic acid, used in the derivatization of alcohols and amines. One class of acetylation reactions are esterification, for example the reaction with ethanol to produce ethyl acetate and hydrogen chloride: CH 3 COCl + HO−CH 2 −CH 3 → CH 3 −COO−CH 2 −CH 3 + HCl

  7. Acyl chloride - Wikipedia

    en.wikipedia.org/wiki/Acyl_chloride

    Acid chlorides are useful for the preparation of amides, esters, anhydrides. These reactions generate chloride, which can be undesirable.Acyl chlorides are used to prepare acid anhydrides, amides and esters, by reacting acid chlorides with: a salt of a carboxylic acid, an amine, or an alcohol, respectively.

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    Get AOL Mail for FREE! Manage your email like never before with travel, photo & document views. Personalize your inbox with themes & tabs. You've Got Mail!

  9. BOP reagent - Wikipedia

    en.wikipedia.org/wiki/BOP_reagent

    [1] [2] It can be prepared from 1-hydroxybenzotriazole and a chlorophosphonium reagent under basic conditions. [3] This reagent has advantages in peptide synthesis since it avoids side reactions like the dehydration of asparagine or glutamine redisues. [4] BOP has used for the synthesis of esters from the carboxylic acids and alcohols. [5]