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4- butyne

The higher homologues of propyne, e.g. 1-decyne, can be obtained in a similar way. Starting from 1-butyne and its homologues, alkylation with alkyl halides leads to 1-alkynes with a branched substituent. [Pg.49]

Give the structures of three isomeric dibromides that could be used as starting materials for the preparation of 3 3 dimethyl 1 butyne J... [Pg.373]

Substituents affect the heats of hydrogenation of alkynes m the same way they affect alkenes Compare the heats of hydrogenation of 1 butyne and 2 butyne both of which give butane on taking up two moles of H2... [Pg.374]

CHsCHjCHzC CH (1 pentyne) CHsCHjC CCHs (2 pentyne) (CH3)2CHC=CH (3 methyl 1 butyne)... [Pg.1214]

Since 1-ethoxy-1-butyne is very volatile, extreme care should be taken during the work-up to minimize loss of product due to evaporation. Extractions especially should be accompanied by careful and frequent venting of the separatory funnel to prevent excessive pressure. [Pg.67]

C4H6 1-BUTYNE (ETHYL- 164.525 1.1892E-01 2.1726E-05 202.09 PHENE ... [Pg.378]


See other pages where 4- butyne is mentioned: [Pg.183]    [Pg.420]    [Pg.421]    [Pg.422]    [Pg.423]    [Pg.24]    [Pg.25]    [Pg.51]    [Pg.74]    [Pg.218]    [Pg.229]    [Pg.364]    [Pg.369]    [Pg.371]    [Pg.373]    [Pg.373]    [Pg.374]    [Pg.374]    [Pg.382]    [Pg.383]    [Pg.383]    [Pg.383]    [Pg.1193]    [Pg.1193]    [Pg.284]    [Pg.287]    [Pg.400]    [Pg.408]    [Pg.517]    [Pg.542]    [Pg.564]    [Pg.586]    [Pg.675]    [Pg.819]    [Pg.823]    [Pg.251]    [Pg.65]    [Pg.66]    [Pg.67]    [Pg.35]    [Pg.364]    [Pg.371]    [Pg.373]   
See also in sourсe #XX -- [ Pg.364 , Pg.371 ]




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1,3-Butadiene with butyne

1,3-Butadiene, 2,3-bis[ -2-butyne

1,4-Dichloro-2-butyne

1- Butyne boiling point

1- Butyne isomerization

1- Butyne photolysis

1- Butyne preparation

1- Butyne synthesis

1- Butyne, 1-ethoxy

1- Butyne, 1-trimethylsilyldeprotonation formation of organolithium reagent from

1- Butyne, 3,3-dimethyl-, mercury-molybdenum-ruthenium complexes

1- Butyne, 715 table

1- ETHOXY-l-BUTYNE

1- phenyl-2-butyne

1-Butyne, hydrogenation over

1-Trimethylsilyl-l-butyne

1.4- Disubstituted 2-butynes

2- BUTYNE-1,4-DIOL.242(Vol

2- Butyn-1,4-diol

2- Butynal

2- Butynal

2- Butyne 1.4- diphenyl

2- Butyne hydration

2- Butyne reaction with iron carbene complexes

2- Butyne transition metal complexes

2- Butyne, bond distances

2- Butyne, l,4-bis reaction with Eschenmoser’s salt

2- Methyl-3-butyn reaction

2- Methyl-3-butyn synthesis

2- butyne-l,4-diol

2-Butyn

2-Butyn

2-Butyne Butyric acid

2-Butyne hydrogenation to cis-2-butene

2-Butyne, 1,4-dibromo

2-Butyne, 1,4-dichlororeaction with bromine

2-Butyne, cobalt-molybdenum-ruthenium

2-Butyne, cobalt-molybdenum-ruthenium complexes

2-Butyne, reaction with chlorine to give

2-Butyne-l,4-diol diacetate

2-Ethyl-3-butyn

2-Methyl-3-butyn

2-acetoxy-2-methyl-3-butyne

2-butyne, cycloaddition

2-butyne, reaction

3 Butyn 2 ol, 2-methyl

3- Butyn-2-one

3- Butyn-l-ols

3- Butyn-l-yl trifluoromethanesulfonate

3- Butyne-2-one

3- Chloro-3-methyl-l-butyne

3- METHYL-1-BUTYNE.24(Vol

3- Methyl-l-butyn

3- methyl-1-butyne

3-Butyn-2-ol, 4-

3-Butyne Subject

3-Methyl-3-hydroperoxy-l-butyne

3-Methyl-3-hydroperoxy-l-butyne Acetylene Hydroperoxides

3-Methyl-l-butyne

3-chloro-1 -butyne

3.3- difluoro-l-butyne

3.3- dimethyl-l-butyne

4-Dimethylamino-3-butyne-2-one

4-Methoxycarbonyloxy-2-butyn

Bis -2-butyne reaction with

Butane from 2-butyne

Butene, 3,4-dichloro butyn

Butenone 2-Butyne

Butyn Butyrolactone

Butyn-2-ol, 4-(Trimethylsilyl)

Butyn-l-ol

Butyne diol derivatives

Butyne, addition reaction

Butyne, formulas

Butyne-1, hydrogenation

Butyne-1,4-diol

Butyne-1,4-dlol

Butynes

Butynes 2-butyne

Butynes butynediol

Butynes living polymerization

Butynes, hydrogenation

Butynes. Diels-Alder with

Butyns-1,4-diol

C4H5F 4-Fluoro-l-butyne

Chlorine, reaction with 2-butyne

Chloro-l-butyne

C«H. 1-Butyne

Dimethoxy-2-butyne

F 1-Butyne

Hexafluoro 2-butyne by photolysis

Hexafluoro-2-butyne

Hexafluoro-2-butyne cycloadditions

Hexafluoro-2-butyne, reaction with

Hexafluoro-2-butyne, transition metal

Hexafluoro-2-butyne, transition metal complexes

Hexakis -2-butyne

Hydrogenation 2-methyl-3-butyne

Hydrogenation of 2-butyne-l ,4-diol

L,4-Dichloro-2-butyne

L-Butyn

L-Butyne,3,3-dimethyl-, mercury-molybdenum-ruthenium complexes

Living polymerization of 2-butyne

Methylenomycin 2-butyne acylation

Perfluoro-2-butyne

Perfluoro-2-butyne, reaction

Perfluoro-3-methyl-l-butyne

Phenyl-l-butyne

Physical Properties of 2-Butyne-1,4—diol

Synthesis of Enantiopure 3-Butyn-2-ol

The Butynes

Triethoxy-2--butyne

Trimethylsilyl-3-butyn

Trimethylsilyl-4-bromomagnesio-l-butyne

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