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  2. 2,2,4,4-Tetramethyl-3-t-butyl-pentane-3-ol - Wikipedia

    en.wikipedia.org/wiki/2,2,4,4-Tetramethyl-3-t...

    2,2,4,4-Tetramethyl-3-t-butyl-pentane-3-ol or tri-tert-butylcarbinol is an organic compound with formula C 13 H 28 O, ((H 3 C) 3 C) 3 COH, or t Bu 3 COH. [1] It is an alcohol that can be viewed as a structural analog of a tridecane isomer ( 2,2,4,4-tetramethyl-3- t -butylpentane ) where the central hydrogen has been replaced by a hydroxyl group ...

  3. Rate-determining step - Wikipedia

    en.wikipedia.org/wiki/Rate-determining_step

    NO 3 + CO → NO 2 + CO 2 (fast step) In this mechanism the reactive intermediate species NO 3 is formed in the first step with rate r 1 and reacts with CO in the second step with rate r 2. However, NO 3 can also react with NO if the first step occurs in the reverse direction (NO + NO 32 NO 2) with rate r −1, where the minus sign ...

  4. Triphenylmethane - Wikipedia

    en.wikipedia.org/wiki/Triphenylmethane

    Triphenylmethane or triphenyl methane (sometimes also known as Tritan), is the hydrocarbon with the formula (C 6 H 5) 3 CH. This colorless solid is soluble in nonpolar organic solvents and not in water.

  5. Aldol reaction - Wikipedia

    en.wikipedia.org/wiki/Aldol_reaction

    [2] [3] [4] The aldol reaction is paradigmatic in organic chemistry and one of the most common means of forming carbon–carbon bonds in organic chemistry . [ 5 ] [ 6 ] [ 7 ] It lends its name to the family of aldol reactions and similar techniques analyze a whole family of carbonyl α-substitution reactions , as well as the diketone ...

  6. Standard step method - Wikipedia

    en.wikipedia.org/wiki/Standard_Step_Method

    To find the length of the gradually varied flow transitions, iterate the “step length”, instead of height, at the boundary condition height until equations 4 and 5 agree. (e.g. For an M1 Profile, position 1 would be the downstream condition and you would solve for position two where the height is equal to normal depth.)

  7. Reaction intermediate - Wikipedia

    en.wikipedia.org/wiki/Reaction_intermediate

    This forms a carbocation intermediate, and the X then bonds to the positive carbon that is available, as in the following two-step reaction. [4] CH 2 CH 2 + HX → CH 2 CH + 3 + X − CH 2 CH + 3 + X − → CH 2 XCH 3. Similarly, in an H 2 O addition reaction, the pi bond of an alkene acts as a nucleophile and bonds with the proton of an [H 3 ...

  8. Single displacement reaction - Wikipedia

    en.wikipedia.org/wiki/Single_displacement_reaction

    The activity series for halogens is: [1] [2] [3] > > > Due to the free state nature of and , single displacement reactions are also redox reactions, involving the transfer of electrons from one reactant to another. [4]

  9. Step-growth polymerization - Wikipedia

    en.wikipedia.org/wiki/Step-growth_polymerization

    The equation above can also be used for a monofunctional additive which is the following, = (+) where N B is the number of monofunction molecules added. The coefficient of 2 in front of N B is require since one B molecule has the same quantitative effect as one excess B-B molecule. [15]

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