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  2. Acetonitrile - Wikipedia

    en.wikipedia.org/wiki/Acetonitrile

    Acetonitrile is used mainly as a solvent in the purification of butadiene in refineries. Specifically, acetonitrile is fed into the top of a distillation column filled with hydrocarbons including butadiene, and as the acetonitrile falls down through the column, it absorbs the butadiene which is then sent from the bottom of the tower to a second separating tower.

  3. Ruthenium(III) acetylacetonate - Wikipedia

    en.wikipedia.org/wiki/Ruthenium(III)_acetylacetonate

    Ruthenium(III) acetylacetonate is a coordination complex with the formula Ru(O 2 C 5 H 7) 3. O 2 C 5 H 7 − is the ligand called acetylacetonate. This compound exists as a dark red solid that is soluble in most organic solvents. [3] It is used as a precursor to other compounds of ruthenium.

  4. Tetrakis(acetonitrile)copper(I) hexafluorophosphate - Wikipedia

    en.wikipedia.org/wiki/Tetrakis(acetonitrile...

    Tetrakis(acetonitrile)copper(I) hexafluorophosphate is a salt with the formula [Cu(CH 3 CN) 4]PF 6. It is a colourless solid that is used in the synthesis of other copper complexes. The cation [Cu(CH 3 CN) 4] + is a well-known example of a transition metal nitrile complex. [1]

  5. Electron configurations of the elements (data page) - Wikipedia

    en.wikipedia.org/wiki/Electron_configurations_of...

    As an approximate rule, electron configurations are given by the Aufbau principle and the Madelung rule. However there are numerous exceptions; for example the lightest exception is chromium, which would be predicted to have the configuration 1s 2 2s 2 2p 6 3s 2 3p 6 3d 4 4s 2 , written as [Ar] 3d 4 4s 2 , but whose actual configuration given ...

  6. Acetyl cyanide - Wikipedia

    en.wikipedia.org/wiki/Acetyl_cyanide

    Two main types of reactions can occur with acetyl cyanide as a reactant; aldol condensation and enolate substitution. Aldol condensation can occur when acetyl cyanide reacts with (Z)-but-2-enal to form (2E,4E)-hexa-2,4-dienoyl cyanide:

  7. Chloroacetonitrile - Wikipedia

    en.wikipedia.org/wiki/Chloroacetonitrile

    Chloroacetonitrile is the organic compound with the formula ClCH 2 CN. A colorless liquid, it is derived from acetonitrile (CH 3 CN) by replacement of one H with Cl. In practice, it is produced by dehydration of chloroacetamide. [1] The compound is an alkylating agent, [2] and as such is handled cautiously.

  8. Trigonal pyramidal molecular geometry - Wikipedia

    en.wikipedia.org/wiki/Trigonal_pyramidal...

    This would result in the geometry of a regular tetrahedron with each bond angle equal to arccos(− ⁠ 1 / 3 ⁠) ≈ 109.5°. However, the three hydrogen atoms are repelled by the electron lone pair in a way that the geometry is distorted to a trigonal pyramid (regular 3-sided pyramid) with bond angles of 107°.

  9. Transition metal nitrile complexes - Wikipedia

    en.wikipedia.org/wiki/Transition_metal_nitrile...

    Typical nitrile ligands are acetonitrile, propionitrile, and benzonitrile.The structures of [Ru(NH 3) 5 (NCPh)] n+ have been determined for the 2+ and 3+ oxidation states. Upon oxidation the Ru-NH 3 distances contract and the Ru-NCPh distances elongate, consistent with amines serving as pure-sigma donor ligands and nitriles functioning as pi-acceptors.