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  2. Carbamic acid - Wikipedia

    en.wikipedia.org/wiki/Carbamic_acid

    Carbamic acid is a planar molecule. [3]The H 2 N− group of carbamic acid, unlike that of most amines, cannot be protonated to an ammonium group H 3 N + −.The zwitterionic form H 3 N + −COO − is very unstable and promptly decomposes into ammonia and carbon dioxide, [6] yet there is a report of its detection in ices irradiated with high-energy protons.

  3. Phenylboronic acid - Wikipedia

    en.wikipedia.org/wiki/Phenylboronic_acid

    Phenylboronic acid or benzeneboronic acid, abbreviated as PhB(OH) 2 where Ph is the phenyl group C 6 H 5 - and B(OH) 2 is a boronic acid containing a phenyl substituent and two hydroxyl groups attached to boron. Phenylboronic acid is a white powder and is commonly used in organic synthesis.

  4. Protodeboronation - Wikipedia

    en.wikipedia.org/wiki/Protodeboronation

    In fact, the addition of acid (H+) or hydroxide (OH-) acts to attenuate protodeboronation by shifting the speciation away from the reactive zwitterion. It is important to note that not all basic heteroaromatic boronic acids are reactive through a zwitterionic intermediate. Scheme for the speciation of 2-pyridine boronic acid in aqueous solution

  5. Carbamate - Wikipedia

    en.wikipedia.org/wiki/Carbamate

    In water solutions, the carbamate anion slowly equilibrates with the ammonium NH + 4 cation and the carbonate CO 2− 3 or bicarbonate HCO − 3 anions: [3] [4] [5] H 2 NCO − 2 + 2 H 2 O ⇌ NH + 4 + HCO − 3 + OH − H 2 NCO − 2 + H 2 O ⇌ NH + 4 + CO 2− 3. Calcium carbamate is soluble in water, whereas calcium carbonate is not.

  6. tert-Butyloxycarbonyl protecting group - Wikipedia

    en.wikipedia.org/wiki/Tert-butyloxycarbonyl...

    Removal of the BOC group in amino acids can be accomplished with strong acids such as trifluoroacetic acid in dichloromethane, or with HCl in methanol. [ 2 ] [ 3 ] [ 4 ] A complication may be the tendency of the t -butyl cation intermediate to alkylate other nucleophiles; scavengers such as anisole or thioanisole may be used.

  7. Perfluoroalkyl carboxylic acids - Wikipedia

    en.wikipedia.org/.../Perfluoroalkyl_carboxylic_acids

    Trifluoroacetic acid is a widely employed acid, used for example in the synthesis of peptides.Its esters are useful in analytical chemistry. Longer-chain perfluoroalkyl carboxylic acids, e.g. with five to nine carbons, are useful fluorosurfactants and emulsifiers used in the production of polytetrafluoroethylene (Teflon) and related fluoropolymers.

  8. It is possible to enjoy the holidays while maintaining a healthy lifestyle, says Dr. Nicole Saphier. The Fox News medical contributor shares her tips for navigating the season in a nutritious way.

  9. Perfluorinated compound - Wikipedia

    en.wikipedia.org/wiki/Perfluorinated_compound

    Many perfluorinated compounds have properties that are quite different from their C-H containing analogues. Common functional groups in PFCs are OH, CO 2 H, chlorine, O, and SO 3 H. Electrofluorination is the predominant method for PFC production. Due to their chemical stability, some of these perfluorinated compounds bioaccumulate.