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  2. Nucleophilic substitution - Wikipedia

    en.wikipedia.org/wiki/Nucleophilic_substitution

    Aprotic solvents do not add protons (H + ions) into solution; if protons were present in S N 2 reactions, they would react with the nucleophile and severely limit the reaction rate. Since this reaction occurs in one step, steric effects drive the reaction speed. In the intermediate step, the nucleophile is 185 degrees from the leaving group and ...

  3. File:Organic Chemistry.pdf - Wikipedia

    en.wikipedia.org/wiki/File:Organic_Chemistry.pdf

    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.

  4. Glycol cleavage - Wikipedia

    en.wikipedia.org/wiki/Glycol_cleavage

    Glycol cleavage is a specific type of organic chemistry oxidation. The carbon–carbon bond in a vicinal diol (glycol) is cleaved and instead the two oxygen atoms become double-bonded to their respective carbon atoms. Depending on the substitution pattern in the diol, these carbonyls will be ketones and/or aldehydes. [1]

  5. Reaction mechanism - Wikipedia

    en.wikipedia.org/wiki/Reaction_mechanism

    In chemistry, a reaction mechanism is the step by step sequence of elementary reactions by which overall chemical reaction occurs. [1]A chemical mechanism is a theoretical conjecture that tries to describe in detail what takes place at each stage of an overall chemical reaction.

  6. List of water-miscible solvents - Wikipedia

    en.wikipedia.org/wiki/List_of_water-miscible...

    Download as PDF; Printable version; In other projects Wikidata item; Appearance. ... Organic compounds. Chemical formula Name CAS number CH 3 CHO: acetaldehyde: 75-07-0

  7. Corey–House synthesis - Wikipedia

    en.wikipedia.org/wiki/Corey–House_synthesis

    The Corey–House synthesis (also called the Corey–Posner–Whitesides–House reaction and other permutations) is an organic reaction that involves the reaction of a lithium diorganylcuprate with an organic halide or pseudohalide (′) to form a new alkane, as well as an ill-defined organocopper species and lithium (pseudo)halide as byproducts.

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  9. Theta solvent - Wikipedia

    en.wikipedia.org/wiki/Theta_solvent

    In a polymer solution, a theta solvent (or θ solvent) is a solvent in which polymer coils act like ideal chains, assuming exactly their random walk coil dimensions. [ clarification needed ] Therefore, the Mark–Houwink equation exponent is 1 / 2 {\displaystyle 1/2} in a theta solvent.