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The Pourbaix diagram for chromium in pure water, perchloric acid, or sodium hydroxide [1] [2] Chromium compounds are compounds containing the element chromium (Cr). Chromium is a member of group 6 of the transition metals. The +3 and +6 states occur most commonly within chromium compounds, followed by +2; charges of +1, +4 and +5 for chromium ...
The systematic IUPAC name is not always the preferred IUPAC name, for example, lactic acid is a common, and also the preferred, name for what systematic rules call 2-hydroxypropanoic acid. This list is ordered by the number of carbon atoms in a carboxylic acid.
Chromium(III) hydroxide (Cr(OH) 3) is amphoteric, dissolving in acidic solutions to form [Cr(H 2 O) 6] 3+, and in basic solutions to form [Cr(OH) 6] 3−. It is dehydrated by heating to form the green chromium(III) oxide (Cr 2 O 3), a stable oxide with a crystal structure identical to that of corundum. [21]
Chromium(III) hydroxide is a gelatinous green inorganic compound with the chemical formula Cr(OH) 3. It is a polymer with an undefined structure and low solubility. It is amphoteric, dissolving in both strong alkalis and strong acids. [2] In alkali: Cr(OH) 3 + OH − → CrO − 2 + 2 H 2 O In acid: Cr(OH) 3 (OH 2) 3 + 3 H + → Cr(OH 2) 6 3+
Formic acid (HCO 2 H) 3.75 Chloroformic acid (ClCO 2 H) 0.27 [5] Acetic acid (CH 3 CO 2 H) 4.76 Glycine (NH 2 CH 2 CO 2 H) 2.34 Fluoroacetic acid (FCH 2 CO 2 H) 2.586 Difluoroacetic acid (F 2 CHCO 2 H) 1.33 Trifluoroacetic acid (CF 3 CO 2 H) 0.23 Chloroacetic acid (ClCH 2 CO 2 H) 2.86 Dichloroacetic acid (Cl 2 CHCO 2 H) 1.29 Trichloroacetic ...
The joining of two aldehyde sugars to form a disaccharide removes the −OH from the carboxy group at the aldehyde end of one sugar. The creation of a peptide bond to link two amino acids to make a protein removes the −OH from the carboxy group of one amino acid. [citation needed]
Chromium trioxide is the anhydride of molecular chromic acid. It is a Lewis acid and can react with a Lewis base, such as pyridine in a non-aqueous medium such as dichloromethane (Collins reagent). Structure of tetrachromic acid H 2 Cr 4 O 13 ·2H 2 O, one component of concentrated "chromic acid". The H-atom positions are calculated, not observed.
In organic chemistry, a sugar acid or acidic sugar is a monosaccharide with a carboxyl group at one end or both ends of its chain. [ 1 ] Main classes of sugar acids include: