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Alkynes molecular formula

Alkene Molecular Formula Alkyne Molecular Formula... [Pg.203]

The classes of hydrocarbons are alkanes, alkenes, alkynes, and arenes Alkanes are hydrocarbons in which all of the bonds are single bonds and are characterized by the molecular formula C H2 +2... [Pg.95]

Hydrocarbons that contain a carbon-carbon triple bond are called alkynes Non cyclic alkynes have the molecular formula C H2 -2 Acetylene (HC=CH) is the simplest alkyne We call compounds that have their triple bond at the end of a carbon chain (RC=CH) monosubstituted or terminal alkynes Disubstituted alkynes (RC=CR ) have internal triple bonds You will see m this chapter that a carbon-carbon triple bond is a functional group reacting with many of the same reagents that react with the double bonds of alkenes... [Pg.363]

Which of the alkynes of molecular formula CsHs can be prepared... [Pg.372]

Wnte structural formulas for all the alkynes of molecular formula CgHi4 that yield 3 ethyl hexane on catalytic hydrogenation... [Pg.386]

Try making a model of a hydrocarbon that contains three carbons only one of which is sp hybridized What is its molecular formula Is it an alkyne" What must be the hybridization state of the other two carbons (You will learn more about compounds of this type in Chapter 10 )... [Pg.389]

The classification of hydrocarbons as aliphatic or aromatic took place m the 1860s when It was already apparent that there was something special about benzene toluene and their derivatives Their molecular formulas (benzene is CgHg toluene is C7Hj ) indicate that like alkenes and alkynes they are unsaturated and should undergo addition reac tions Under conditions m which bromine for example reacts rapidly with alkenes and alkynes however benzene proved to be inert Benzene does react with Bi2 m the pres ence of iron(III) bromide as a catalyst but even then addition isn t observed Substitu tion occurs instead ... [Pg.424]

Which of the alkynes of molecular formula CsHs can be prepared in good yield by alkylation or dialkylation of acetylene Explain why the preparation of the other CsHg isomers would not be practical. [Pg.372]

Give the molecular formula and identify each of the following molecules as being an alkane, alkene, or alkyne ... [Pg.867]

Give the molecular formulas corresponding to the following stick figures and identify each as an alkane, an alkene, an alkyne, or an aromatic hydrocarbon ... [Pg.867]

The empirical formula is C4Hy the molecular formula might be C jHlg, which matches the formula for alkanes (C H, +,). It is not likely an alkene or alkyne, because there is no reasonable Lewis structure for a compound having the empirical formula C4II9 and multiple bonds. [Pg.1023]

Figure 8.4 The v = 6 C-H overtone spectrum as determined by photoacoustic absorption (Hall, 1984) for increasing size alkynes. Each panel contains the molecular formula and the density of vibrational states per cm 1. The band origin does shift some with size but is roughly at 18450 cm"1 for all the molecules shown (see also Kerstel et al., 1991). Figure 8.4 The v = 6 C-H overtone spectrum as determined by photoacoustic absorption (Hall, 1984) for increasing size alkynes. Each panel contains the molecular formula and the density of vibrational states per cm 1. The band origin does shift some with size but is roughly at 18450 cm"1 for all the molecules shown (see also Kerstel et al., 1991).
Problem 8.2 Supply structural formulas and lUPAC names for all alkynes with the molecular formula a) C,H , b) C,H, . ... [Pg.142]

Aromatic carbon-carbon bonds are intermediate in length (139 pm) between that of a C—C single bond (154 pm) and a C—C double bond (134 pm). An aromatic ring is characterized by a delocalized r system in contrast to the localized bonds present in aliphatic hydrocarbons. 18.65 The empirical formula is C2H5. The compound is an alkane the molecular formula might be C4H10, which matches the formula for alkanes (C H2n + 2). It is not an alkene or alkyne, because they both have (mole H) (mole C) ratios less than 2.5. [Pg.1089]

Ethynylcyclohexane has the molecular formula C8H12. All the other compounds are Only alkynes with the carbon skeletons shown can give 3-ethylhexane on catalytic... [Pg.215]

Compounds of molecular formula CUH20 have two double bonds or one triple bond. The only compounds with the proper carbon skeleton are the alkyne and the allene shown. [Pg.238]

Alkenes are said to be unsaturated because they are capable of adding hydrogen in the presence of a catalyst. The product, an alkane, is called saturated because it cannot react with any more hydrogen. The presence of a pi bond of an alkene (or an alkyne) or the ring of a cyclic compound decreases the number of hydrogen atoms in a molecular formula. These structural features are called elements of unsaturation. Each element of unsaturation corresponds to two fewer hydrogen atoms than in the saturated formula. [Pg.287]

A triple bond gives an alkyne four fewer hydrogens than the corresponding alkane. Its molecular formula is like that of a molecule with two double bonds CnH2n-2-Therefore, the triple bond contributes two elements of unsaturation (eu) (Section 7-3). [Pg.392]

For each molecular formula, draw all the isomeric alkynes, and give their IUPAC names. Circle the acetylenic hydrogen of each terminal alkyne. [Pg.394]

Deduce the structure of an alkene or alkyne from its molecular formula and products of cleavage. [Pg.182]

What is the molecular formula of an alkyne of which 0.63 grams contains 0.07 grams of H ... [Pg.102]

An alkyne is a hydrocarbon with one carbon-to-carbon triple bond per molecule. The series has molecules with the general molecular formula C H2 2- The first alkyne, called ethyne and commonly known as acetylene, has the formula C2H2 or HC=CH, also written CH CH. Acetylene is used as a fuel in high-temperature welding torches. The alkynes are named similarly to the alkanes and alkenes, but with the ending -yne. [Pg.537]


See other pages where Alkynes molecular formula is mentioned: [Pg.364]    [Pg.189]    [Pg.364]    [Pg.940]    [Pg.160]    [Pg.596]    [Pg.370]    [Pg.9]    [Pg.1023]    [Pg.189]    [Pg.6]    [Pg.393]    [Pg.140]    [Pg.4]    [Pg.103]    [Pg.103]    [Pg.103]   
See also in sourсe #XX -- [ Pg.98 , Pg.131 ]

See also in sourсe #XX -- [ Pg.400 ]




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