Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Basicity Charge-assisted hydrogen bonds

Tertiary alkyl chlorides are easily dehydrochlorinated by base (via the E2, or bimolecular elimination reaction mechanism), but the environment of the degrading resin is not basic. Loss of hydrogen chloride to yield an olefin can occur principally by the El, or monomolecular elimination reaction. This is a slow reaction because, in the rate-determining step, the C—Cl bond is broken to form two separated oppositely charged particles. The reaction rate is not assisted by the acid present. [Pg.47]


See other pages where Basicity Charge-assisted hydrogen bonds is mentioned: [Pg.64]    [Pg.589]    [Pg.30]    [Pg.555]    [Pg.162]    [Pg.308]    [Pg.6]    [Pg.12]    [Pg.269]    [Pg.57]    [Pg.235]    [Pg.586]    [Pg.130]    [Pg.150]    [Pg.23]    [Pg.161]    [Pg.61]   
See also in sourсe #XX -- [ Pg.12 ]




SEARCH



Basicity, hydrogen bonding

Bonding basics

Charge bond

Hydrogen basicity

Hydrogen bond basicity

Hydrogen bond charge-assisted

Hydrogen bonding charge-assisted

Hydrogen charging

© 2024 chempedia.info