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Isobutanal

Alkylation is a process that produces high octane number (RON and MON) components from light olefins ( 3=, 4=, 05=) by addition of isobutane. [Pg.373]

We cite isomerization of Cs-Ce paraffinic cuts, aliphatic alkylation making isoparaffinic gasoline from C3-C5 olefins and isobutane, and etherification of C4-C5 olefins with the C1-C2 alcohols. This type of refinery can need more hydrogen than is available from naphtha reforming. Flexibility is greatly improved over the simple conventional refinery. Nonetheless some products are not eliminated, for example, the heavy fuel of marginal quality, and the conversion product qualities may not be adequate, even after severe treatment, to meet certain specifications such as the gasoline octane number, diesel cetane number, and allowable levels of certain components. [Pg.485]

Solve the same problem for propane and isobutane (2-methylpropane). The bond matrix is the same as it is for n-butane, but the enthalpy of formation is somewhat different (n-butane) = —127.1 kJ mol vs. (isobutane) = —134.2... [Pg.56]

Alkylation combines lower-molecular-weight saturated and unsaturated hydrocarbons (alkanes and alkenes) to produce high-octane gasoline and other hydrocarbon products. Conventional paraffin-olefin (alkane-alkene) alkylation is an acid-catalyzed reaction, such as combining isobutylene and isobutane to isooctane. [Pg.102]

Alkylation of isoalkanes with alkenes is of particular significance. The industrially used alkylation of isobutane with isobutylene to iso-... [Pg.164]

These are effective high-octane gasoline additive oxygenates. The conversion of isobutane into isopropyl, methyl ketone, or isopentane into isobutyl, methyl ketone is illustrative. In this reaction, no branched carboxylic acids (Koch products) are formed. [Pg.166]

Because the protonation of ozone removes its dipolar nature, the electrophilic chemistry of HOs, a very efficient oxygenating electrophile, has no relevance to conventional ozone chemistry. The superacid-catalyzed reaction of isobutane with ozone giving acetone and methyl alcohol, the aliphatic equivalent of the industrially significant Hock-reaction of cumene, is illustrative. [Pg.166]

Carboxoninm ions, for example, do not react with alkanes. However, in superacid solution acetaldehyde (or acetone), for example, readily reacts with isobutane involving diprotonated, highly reactive carbocationic species. [Pg.195]

Methane is the only alkane of molecular formula CH4 ethane the only one that is C2H6 and propane the only one that is C3Hj Beginning with C4H10 however constitutional isomers (Section 1 8) are possible two alkanes have this particular molecular formula In one called n butane, four carbons are joined m a continuous chain The nmn butane stands for normal and means that the carbon chain is unbranched The second isomer has a branched carbon chain and is called isobutane... [Pg.67]

As just noted (Section 2 7) CH3 is called a methyl group In addition to having methyl groups at both ends n butane contains two CH2 or methylene groups Isobutane con tains three methyl groups bonded to a CH unit The CH unit is called a methme group... [Pg.67]

Butane lighters contain about 5% n butane and 95% isobutane in a sealed con tamer The pressure pro duced by the two com pounds (about 3 atm) is enough to keep them in the liquid state until opening a small valve emits a fine stream of the vaporized mixture across a spark which ignites it... [Pg.68]

Bonding m n butane and isobutane continues the theme begun with methane ethane and propane All of the carbon atoms are sp hybridized all of the bonds are ct bonds and the bond angles at carbon are close to tetrahedral This generalization holds for all alkanes regardless of the number of carbons they have... [Pg.68]

The C4H9 alkyl groups may be derived either from the unbranched carbon skele ton of butane or from the branched carbon skeleton of isobutane Those derived from butane are the butyl (n butyl) group and the 1 methylpropyl (sec butyl) group... [Pg.74]

Those derived from isobutane are the 2 methylpropyl (isobutyl) group and the 1 1 dimethylethyl (tert butyl) group Isobutyl is a primary alkyl group because its poten tial point of attachment is to a primary carbon tert Butyl is a tertiary alkyl group because Its potential point of attachment is to a tertiary carbon... [Pg.74]

Two constitutionally isomeric alkanes have the molecular formula C4H10 One has an unbranched chain (CH3CH2CH2CH3) and is called n butane, the other has a branched chain [(CH3)3CH] and is called isobutane Both n butane and isobutane are common names... [Pg.96]

Constitutional isomers (Section 1 8) Isomers that differ in re spect to the order in which the atoms are connected Butane (CH3CH2CH2CH3) and isobutane [(CH3)3CH] are constitu tional isomers... [Pg.1280]

Ionization energy (Section 1 2) Amount of energy required to remove an electron from some species Isobutane (Section 2 8) The common name for 2 methyl propane (CH3)3CH... [Pg.1287]

To find Kovat s retention index for isobutane, we use equation 12.29. [Pg.575]


See other pages where Isobutanal is mentioned: [Pg.71]    [Pg.71]    [Pg.224]    [Pg.4]    [Pg.183]    [Pg.375]    [Pg.662]    [Pg.160]    [Pg.466]    [Pg.57]    [Pg.154]    [Pg.165]    [Pg.194]    [Pg.67]    [Pg.68]    [Pg.70]    [Pg.73]    [Pg.101]    [Pg.2]    [Pg.503]    [Pg.523]    [Pg.573]    [Pg.575]    [Pg.575]    [Pg.575]    [Pg.114]    [Pg.528]    [Pg.528]    [Pg.528]    [Pg.7]   
See also in sourсe #XX -- [ Pg.13 , Pg.64 ]

See also in sourсe #XX -- [ Pg.48 ]




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