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Methylpropanal

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]

Similarly by comparing the bond dissociation energies of the two different types of C—H bonds m 2 methylpropane we see that a tertiary radical is 30 kJ/mol (7 kcal/ mol) more stable than a primary radical... [Pg.170]

A similar study of the chlorination of 2 methylpropane established that a tertiary hydrogen is removed 5 2 times faster than each primary hydrogen... [Pg.177]

The benzyhc position m alkylbenzenes is analogous to the allyhc position m alkenes Thus a benzyhc C—H bond like an allyhc one is weaker than a C—H bond of an alkane as the bond dissociation energies of toluene propene and 2 methylpropane attest... [Pg.439]

Chloro 2 methylpropane Isobutyl chloride or 2 methylpropyl chloride 2 Chloro 2 methylpropane tert Butyl chloride or 1 1 dimethylethyl chloride... [Pg.1205]


See other pages where Methylpropanal is mentioned: [Pg.224]    [Pg.36]    [Pg.73]    [Pg.73]    [Pg.152]    [Pg.170]    [Pg.171]    [Pg.171]    [Pg.171]    [Pg.177]    [Pg.177]    [Pg.177]    [Pg.237]    [Pg.439]    [Pg.445]    [Pg.527]    [Pg.531]    [Pg.593]    [Pg.604]    [Pg.658]    [Pg.705]    [Pg.738]    [Pg.739]    [Pg.744]    [Pg.764]    [Pg.907]    [Pg.1192]    [Pg.1194]    [Pg.1194]    [Pg.1207]    [Pg.291]    [Pg.399]    [Pg.401]    [Pg.409]    [Pg.422]    [Pg.423]    [Pg.423]   


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1 Chloro 2 methylpropane

1 Chloro 2 methylpropane chloride

1,1 -Diphenyl-2-methylpropane

1,1 -difluoro-2-methylpropane

1- Bromo-2-methylpropane

1- Bromo-2-methylpropane, from hydrogen

1- Chloro-2-methylpropane Isobutyl chloride

1- methylpropane lithium

1.2- Dichloro-2-methylpropane

1.2- Epoxy-2-methylpropane

1.2- diamino-2-methylpropane

2 Chloro 2 methylpropane Butyl chloride

2 Methylpropanal acidity

2 Methylpropane

2 Methylpropane

2 Methylpropane acidity

2 Methylpropane carbon

2 Methylpropane chemical shifts

2 Methylpropane chlorination

2 Methylpropane proton

2- -2-methylpropanal, reductive

2- -2-methylpropane sulfonate

2- Chloro-2-methylpropane substitution

2- Chloro-2-methylpropane, solvolysis

2- Nitro-2-methylpropane

2- Phenyl-2-methylpropane

2- fluoro-2-methylpropane

2-Acrylamide-2 -methylpropane sulfonic acid

2-Acrylamide-2 -methylpropane sulfonic acid AMPS)

2-Acrylamido-2-methylpropane sulfonic

2-Acrylamido-2-methylpropane sulfonic acid

2-Amino-2-Methylpropane

2-Bromo-2-methylpropane elimination reaction

2-Ethoxy-2-methylpropan

2-Hydroperoxy-2-methylpropane,

2-Hydroxy-2-methylpropanic acid

2-Methoxy-2-methylpropane

2-Methylpropan

2-Methylpropan

2-Methylpropanal , imine

2-Methylpropane bromination

2-Methylpropane fluorination

2-Methylpropane, isomerization

2-Methylpropane, molecular model

2-Methylpropane-2-thiol

2-Methylpropane-l,3-diol

2-Methylpropane-l-thiol

2-acrylamide-2-methylpropane

2-bromo-2-methylpropane reactions

Acid-Catalyzed Enolization of 2-Methylpropanal

Azo-2-methylpropane

Bond dissociation energy 2 methylpropane

Bond dissociation enthalpy 2-methylpropane

Bromination of 2-methylpropane

C4H.Br 2-Bromo-2-methylpropane

C4H.C1 2-Chloro-2-methylpropane

C4H.I l-Iodo-2-methylpropane

Chlorination of 2-methylpropane

Ethane + propane + 2-methylpropane

Ethyl-2-methylpropane

F 2-Bromo-2-methylpropane

Initiated oxidation 2-methylpropane

Iodo-2-methylpropane

Isobutane 2-Methylpropane

L,2-Epoxy-2-methylpropane

L,3-Dichloro-2-methylpropane

L-Bromo-2-methylpropane

L-Iodo-2-methylpropane

Methyl propanal 2-methylpropanal

Methylpropane properties

Perfluoro-2-methylpropane

Solvolysis of 2-chloro-2-methylpropane

Tert Butyl chloride methylpropane

Thallium 2-methylpropane-2-thiolate

Thallous 2-methylpropane-2-thiolate

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