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  2. File:Non-Programmer's Tutorial for Python 3.pdf - Wikipedia

    en.wikipedia.org/wiki/File:Non-Programmer's...

    You are free: to share – to copy, distribute and transmit the work; to remix – to adapt the work; Under the following conditions: attribution – You must give appropriate credit, provide a link to the license, and indicate if changes were made.

  3. Methenium - Wikipedia

    en.wikipedia.org/wiki/Methenium

    3 CN to form the ion (CH 3) 2 CN +. [5] Upon capture of a low-energy electron (less than 1 eV), it will spontaneously dissociate. [6] It is seldom encountered as an intermediate in the condensed phase. It is proposed as a reactive intermediate that forms upon protonation or hydride abstraction of methane with FSO 3 H-SbF 5.

  4. Matplotlib - Wikipedia

    en.wikipedia.org/wiki/Matplotlib

    Matplotlib (portmanteau of MATLAB, plot, and library [3]) is a plotting library for the Python programming language and its numerical mathematics extension NumPy.It provides an object-oriented API for embedding plots into applications using general-purpose GUI toolkits like Tkinter, wxPython, Qt, or GTK.

  5. Carbocation - Wikipedia

    en.wikipedia.org/wiki/Carbocation

    The IUPAC acknowledges the three divergent definitions of carbonium ion and urges care in the usage of this term. For the remainder of this article, the term carbonium ion will be used in this latter restricted sense, while non-classical carbocation will be used to refer to any carbocation with C–C and/or C–H σ-bonds delocalized by bridging.

  6. Reaction intermediate - Wikipedia

    en.wikipedia.org/wiki/Reaction_intermediate

    E1 and E2 are two different mechanisms for elimination reactions, and E1 involves a carbocation intermediate. In E1, a leaving group detaches from a carbon to form a carbocation reaction intermediate. Then, a solvent removes a proton, but the electrons used to form the proton bond form a pi bond, as shown in the pictured reaction on the right. [4]

  7. Hydrohalogenation - Wikipedia

    en.wikipedia.org/wiki/Hydrohalogenation

    This is due to the abstraction of a hydrogen atom by the alkene from the hydrogen halide (HX) to form the most stable carbocation (relative stability: 3°>2°>1°>methyl), as well as generating a halogen anion. A simple example of a hydrochlorination is that of indene with hydrogen chloride gas (no solvent): [4]

  8. Pyramidal carbocation - Wikipedia

    en.wikipedia.org/wiki/Pyramidal_carbocation

    An example of the monovalent carbocation. A pyramidal carbocation is a type of carbocation with a specific configuration. This ion exists as a third class, besides the classical and non-classical ions. In these ions, a single carbon atom hovers over a four- or five-sided polygon, in effect forming a pyramid. The four-sided pyramidal ion will ...

  9. Elimination reaction - Wikipedia

    en.wikipedia.org/wiki/Elimination_reaction

    The E2 mechanism, where E2 stands for bimolecular elimination, involves a one-step mechanism in which carbon-hydrogen and carbon-halogen bonds break to form a double bond (C=C Pi bond). The specifics of the reaction are as follows: E2 is a single step elimination, with a single transition state.

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