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  2. Lewis structure - Wikipedia

    en.wikipedia.org/wiki/Lewis_structure

    [1] [2] [3] Introduced by Gilbert N. Lewis in his 1916 article The Atom and the Molecule, a Lewis structure can be drawn for any covalently bonded molecule, as well as coordination compounds. [4] Lewis structures extend the concept of the electron dot diagram by adding lines between atoms to represent shared pairs in a chemical bond.

  3. Rubidium chloride - Wikipedia

    en.wikipedia.org/wiki/Rubidium_chloride

    At high temperature and pressure, RbCl adopts the caesium chloride (CsCl) structure (NaCl and KCl undergo the same structural change at high pressures). Here, the chloride ions form a simple cubic arrangement with chloride anions occupying the vertices of a cube surrounding a central Rb +.

  4. Structural formula - Wikipedia

    en.wikipedia.org/wiki/Structural_formula

    Skeletal structural formula of Vitamin B 12.Many organic molecules are too complicated to be specified by a molecular formula.. The structural formula of a chemical compound is a graphic representation of the molecular structure (determined by structural chemistry methods), showing how the atoms are possibly arranged in the real three-dimensional space.

  5. Molecular solid - Wikipedia

    en.wikipedia.org/wiki/Molecular_solid

    The quadrupole-quadrupole interactions between the naphthalene molecules partially guide the organization of the crystal lattice structure. [24] (a) A lewis dot structure artificially colored to provide a qualitative map of where the partial charges exist for the quadrupole. A 3D representation of naphthalene molecules and quadrupole.

  6. Phosphorus triiodide - Wikipedia

    en.wikipedia.org/wiki/Phosphorus_triiodide

    Often the PI 3 is made in situ by the reaction of red phosphorus with iodine in the presence of the alcohol; for example, the conversion of methanol to give iodomethane: [5] PI 3 + 3 CH 3 OH → 3 CH 3 I + " H 3 PO 3 " These alkyl iodides are useful compounds for nucleophilic substitution reactions, and for the preparation of Grignard reagents.

  7. Alcohol (chemistry) - Wikipedia

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

    Those groups can form hydrogen bonds to one another and to most other compounds. Owing to the presence of the polar OH alcohols are more water-soluble than simple hydrocarbons. Methanol, ethanol, and propanol are miscible in water. 1-Butanol, with a four-carbon chain, is moderately soluble.

  8. Tetrahedral molecular geometry - Wikipedia

    en.wikipedia.org/wiki/Tetrahedral_molecular_geometry

    In a tetrahedral molecular geometry, a central atom is located at the center with four substituents that are located at the corners of a tetrahedron.The bond angles are arccos(− ⁠ 1 / 3 ⁠) = 109.4712206...° ≈ 109.5° when all four substituents are the same, as in methane (CH 4) [1] [2] as well as its heavier analogues.

  9. Methanol - Wikipedia

    en.wikipedia.org/wiki/Methanol

    Methanol and its vapours are flammable. Moderately toxic for small animals – Highly toxic to large animals and humans (in high concentrations) – May be fatal/lethal or cause blindness and damage to the liver, kidneys, and heart if swallowed – Toxicity effects from repeated over exposure have an accumulative effect on the central nervous system, especially the optic nerve – Symptoms may ...