Big Chemical Encyclopedia

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

Articles Figures Tables About

Branched chain hydrocarbons, heat formation

Part A of Table 1.4 shows all the acyclic C4-C6 hydrocarbons and a number of the Cg hydrocarbons. A general trend is discernible in the heats of formation data. Branched-chain hydrocarbons are more stable than straight-chain hydrocarbons. For example, the MTf for n-octane is -49.82 kcal/mol, whereas the most highly branched isomer possible, 2,2,3,3-tetramethylbutane, is the most stable of the octanes, with a AH of -53.99 kcal/mol. Similar trends are observed in the other series. [Pg.12]

Hydrocaibons with branched chain Heat of formation of isomet ic hydrocarbon kcals Corresponding normal hydrocarbon Heat of formation of notmal hydrocarbon kcals Difference kcals... [Pg.243]


See other pages where Branched chain hydrocarbons, heat formation is mentioned: [Pg.250]    [Pg.243]    [Pg.243]    [Pg.243]    [Pg.243]    [Pg.274]    [Pg.258]    [Pg.249]    [Pg.544]    [Pg.243]    [Pg.243]    [Pg.6]    [Pg.9]    [Pg.546]    [Pg.585]   
See also in sourсe #XX -- [ Pg.243 ]

See also in sourсe #XX -- [ Pg.243 ]




SEARCH



Branch formation

Branched chain

Branched chain hydrocarbons, heat

Branched-chain hydrocarbons

Chain branching

Chain formation

Formation branching

Formation, heat

Hydrocarbons, branched

© 2024 chempedia.info