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  2. Significant figures - Wikipedia

    en.wikipedia.org/wiki/Significant_figures

    The leftmost or largest digit position among the last significant figures of these terms is the ones place, so the calculated result should also have its last significant figure in the ones place. The rule to calculate significant figures for multiplication and division are not the same as the rule for addition and subtraction.

  3. Quantities, Units and Symbols in Physical Chemistry

    en.wikipedia.org/wiki/Quantities,_Units_and...

    Quantities, Units and Symbols in Physical Chemistry, also known as the Green Book, is a compilation of terms and symbols widely used in the field of physical chemistry. It also includes a table of physical constants , tables listing the properties of elementary particles , chemical elements , and nuclides , and information about conversion ...

  4. Reaction mechanism - Wikipedia

    en.wikipedia.org/wiki/Reaction_mechanism

    Instead, the slow step involves two molecules of NO 2. A possible mechanism for the overall reaction that explains the rate law is: 2 NO 2 → NO 3 + NO (slow) NO 3 + CO → NO 2 + CO 2 (fast) Each step is called an elementary step, and each has its own rate law and molecularity. The sum of the elementary steps gives the net reaction.

  5. SigFig - Wikipedia

    en.wikipedia.org/wiki/Sigfig

    Significant figures, the digits of a number that carry meaning contributing to its measurement resolution Topics referred to by the same term This disambiguation page lists articles associated with the title SigFig .

  6. 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 ...

  7. Arrow pushing - Wikipedia

    en.wikipedia.org/wiki/Arrow_pushing

    Arrow pushing or electron pushing is a technique used to describe the progression of organic chemistry reaction mechanisms. [1] It was first developed by Sir Robert Robinson.In using arrow pushing, "curved arrows" or "curly arrows" are drawn on the structural formulae of reactants in a chemical equation to show the reaction mechanism.

  8. Click chemistry - Wikipedia

    en.wikipedia.org/wiki/Click_chemistry

    Click chemistry is an approach to chemical synthesis that emphasizes efficiency, simplicity, selectivity, and modularity in chemical processes used to join molecular building blocks. It includes both the development and use of "click reactions", a set of simple, biocompatible chemical reactions that meet specific criteria like high yield, fast ...

  9. Acyl group - Wikipedia

    en.wikipedia.org/wiki/Acyl_group

    In chemistry, an acyl group is a moiety derived by the removal of one or more hydroxyl groups from an oxoacid, [1] including inorganic acids. It contains a double-bonded oxygen atom and an organyl group ( R−C=O ) or hydrogen in the case of formyl group ( H−C=O ).