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  2. Methoxyethane - Wikipedia

    en.wikipedia.org/wiki/Methoxyethane

    Methoxyethane, also known as ethyl methyl ether, is a colorless gaseous ether with the formula CH 3 OCH 2 CH 3.Unlike the related dimethyl ether and diethyl ether, which are widely used and studied, this mixed alkyl ether has no current applications.

  3. Intramolecular force - Wikipedia

    en.wikipedia.org/wiki/Intramolecular_force

    Intramolecular forces such as disulfide bonds give proteins and DNA their structure. Proteins derive their structure from the intramolecular forces that shape them and hold them together. The main source of structure in these molecules is the interaction between the amino acid residues that form the foundation of proteins. [ 7 ]

  4. Non-covalent interaction - Wikipedia

    en.wikipedia.org/wiki/Non-covalent_interaction

    Non-covalent interactions can be classified into different categories, such as electrostatic, π-effects, van der Waals forces, and hydrophobic effects. [3] [2] Non-covalent interactions [4] are critical in maintaining the three-dimensional structure of large molecules, such as proteins and nucleic acids.

  5. Intermolecular force - Wikipedia

    en.wikipedia.org/wiki/Intermolecular_force

    The induced dipole forces appear from the induction (also termed polarization), which is the attractive interaction between a permanent multipole on one molecule with an induced (by the former di/multi-pole) 31 on another. [12] [13] [14] This interaction is called the Debye force, named after Peter J. W. Debye.

  6. London dispersion force - Wikipedia

    en.wikipedia.org/wiki/London_dispersion_force

    London dispersion forces (LDF, also known as dispersion forces, London forces, instantaneous dipole–induced dipole forces, fluctuating induced dipole bonds [1] or loosely as van der Waals forces) are a type of intermolecular force acting between atoms and molecules that are normally electrically symmetric; that is, the electrons are ...

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  8. Acetic acid - Wikipedia

    en.wikipedia.org/wiki/Acetic_acid

    acetyl chloride SOCl 2 acetic acid (i) Li[AlH 4], ether (ii) H 3 O + ethanol Two typical organic reactions of acetic acid Acetic acid undergoes the typical chemical reactions of a carboxylic acid. Upon treatment with a standard base, it converts to metal acetate and water. With strong bases (e.g., organolithium reagents), it can be doubly deprotonated to give LiCH 2 COOLi. Reduction of acetic ...

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