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  2. Lead (II) acetate - Wikipedia

    en.wikipedia.org/wiki/Lead(II)_acetate

    Its chemical formula is usually expressed as Pb(CH 3 COO) 2 or Pb(OAc) 2, where Ac represents the acetyl group. Like many other lead compounds, it causes lead poisoning. Lead acetate is soluble in water and glycerin. With water it forms the trihydrate, Pb(OAc) 2 ·3H 2 O, a colourless or white efflorescent monoclinic crystalline substance.

  3. Lead(IV) acetate - Wikipedia

    en.wikipedia.org/wiki/Lead(IV)_acetate

    It is typically prepared by treating of red lead with acetic acid and acetic anhydride (Ac 2 O), which absorbs water. The net reaction is shown: [4] [5] Pb 3 O 4 + 4 Ac 2 O → Pb(OAc) 4 + 2 Pb(OAc) 2. The remaining lead(II) acetate can be partially oxidized to the tetraacetate by Cl 2, with a PbCl 2 by-product: 2 Pb(OAc) 2 + Cl 2Pb(OAc) 4 ...

  4. IUPAC nomenclature of organic chemistry - Wikipedia

    en.wikipedia.org/wiki/IUPAC_nomenclature_of...

    For example, (CH 3) 2 CHCH 3, commonly known as isobutane, is treated as a propane chain with a methyl group bonded to the middle (2) carbon, and given the systematic name 2-methylpropane. However, although the name 2-methylpropane could be used, it is easier and more logical to call it simply methylpropane – the methyl group could not ...

  5. List of Unicode characters - Wikipedia

    en.wikipedia.org/wiki/List_of_Unicode_characters

    A numeric character reference refers to a character by its Universal Character Set/Unicode code point, and a character entity reference refers to a character by a predefined name. A numeric character reference uses the format &#nnnn; or &#xhhhh; where nnnn is the code point in decimal form, and hhhh is the code point in hexadecimal form.

  6. Acetoxy group - Wikipedia

    en.wikipedia.org/wiki/Acetoxy_group

    In organic chemistry, the acetoxy group (abbr. AcO or OAc; IUPAC name: acetyloxy [1]), is a functional group with the formula −OCOCH 3 and the structure −O−C(=O)−CH 3. As the -oxy suffix implies, it differs from the acetyl group (−C(=O)−CH 3) by the presence of an additional oxygen atom. The name acetoxy is the short form of acetyl-oxy.

  7. Glycol cleavage - Wikipedia

    en.wikipedia.org/wiki/Glycol_cleavage

    Iodine-based reagents such as periodic acid (HIO 4) and (diacetoxyiodo)benzene (PhI(OAc) 2) are commonly used. [3] Another reagent is lead tetraacetate (Pb(OAc) 4). [4] These I- and Pb-based methods are called the Malaprade reaction and Criegee oxidation, respectively. The former is favored for aqueous solutions, the latter for nonaqueous ...

  8. Palladium(II) acetate - Wikipedia

    en.wikipedia.org/wiki/Palladium(II)_acetate

    Palladium(II) acetate is a chemical compound of palladium described by the formula [Pd(O 2 CCH 3) 2] n, abbreviated [Pd(OAc) 2] n. It is more reactive than the analogous platinum compound. Depending on the value of n, the compound is soluble in many organic solvents and is commonly used as a catalyst for organic reactions. [2]

  9. Chromium (II) acetate - Wikipedia

    en.wikipedia.org/wiki/Chromium(II)_acetate

    The Cr 2 (OAc) 4 (H 2 O) 2 molecule contains two atoms of chromium, two ligated molecules of water, and four acetate bridging ligands.The coordination environment around each chromium atom consists of four oxygen atoms (one from each acetate ligand) in a square, one water molecule (in an axial position), and the other chromium atom (opposite the water molecule), giving each chromium centre an ...