Hydrogen atom alkenes

Alkanes, with the general formula C H2 +2, are saturated hydrocarbons, in which each carbon atom is singly bonded to four other atoms. These atoms are either carbon atoms or hydrogen atoms. Alkenes, C H2 , and alkynes, C H2 2, are unsaturated hydrocarbons in which there is a carbon-carbon double bond or a carbon-carbon triple bond, respectively. 

Alkenes contain one or more double bonds. Alkenes, alkynes, and aromatics are unsaturated because they have fewer hydrogen atoms.Alkenes are also called olefins. The suffix used in the naming of alkenes is -ene, and the number roots are those used for alkanes of the same length. 

Unsaturated hydrocarbons Hydrocarbons that contain fewer than the maximum number of hydrogen atoms alkenes and alkynes... 

Alkenes and alkynes are classified as unsaturated hydrocarbons. They are said to be unsaturated because, unlike alkanes, their molecules do not contain the maximum possible number of hydrogen atoms. Alkenes have two fewer hydrogen atoms, and alk3mes have four fewer hydrogen atoms than alkanes with a comparable number of carbon atoms. Alkenes contain at least one double bond between adjacent carbon atoms, while alkynes contain at least one triple bond between adjacent carbon atoms. 

MarkownikofT s rule The rule states that in the addition of hydrogen halides to an ethyl-enic double bond, the halogen attaches itself to the carbon atom united to the smaller number of hydrogen atoms. The rule may generally be relied on to predict the major product of such an addition and may be easily understood by considering the relative stabilities of the alternative carbenium ions produced by protonation of the alkene in some cases some of the alternative compound is formed. The rule usually breaks down for hydrogen bromide addition reactions if traces of peroxides are present (anti-MarkownikofT addition). 

Step 4 The second hydrogen atom is transferred forming the alkane The sites on the catalyst surface at which the reaction occurred are free to accept additional hydrogen and alkene molecules... 

In the mechanism for alkene hydrogenation shown m Figure 6 1 hydrogen atoms are transferred from the catalyst s surface to the alkene Although the two hydrogens are not transferred simultaneously they both add to the same face of the double bond... 

What about a substance wrth the molecular formula 71414 Thrs compound can not be an alkane but may be erther a cycloalkane or an alkene because both these classes of hydrocarbons correspond to the general molecular formula C H2 Any time a ring or a double bond is present in an organic molecule its molecular formula has two fewer hydrogen atoms than that of an alkane with the same number of carbons... 

Bivalent radicals derived from unbranched alkenes, alkadienes, and alkynes by removing a hydrogen atom from each of the terminal carbon atoms are named by replacing the endings -ene, -diene, and -yne by -enylene, -dienylene, and -ynylene, respectively. Positions of double and triple bonds are indicated by numbers when necessary. The name vinylene instead of ethenylene is retained for —CH=CH—. 

Hydrochlorination. The addition of hydrogen chloride to alkenes in the absence of peroxides takes place by an electrophilic substitution mechanism. The orientation is in accord -with Markovnikov s mle in -which the hydrogen atom adds to the side of the double bond that -will result in the... 

Diazo compounds react with alkenes to afford A -pyrazolines, which in turn izomerize to A -pyrazolines if there is a hydrogen atom a to the N=N bond (Scheme 54). In those cases where two possible ways of isomerization exist, the more acidic hydrogen migrates preferentially. The alkene configuration is conserved on the A -pyrazoline (stereospecificity) but the regioselectivity depends on the substituents of both the alkene and the diazo compound. 

The bicyclic product is formed by coupling of the two radical sites, while the alkene results from an intramolecular hydrogen-atom transfer. These reactions can be sensitized by aromatic ketones and quenched by typical triplet quenchers and are therefore believed to proceed via triplet excited states. 

Note that these compounds are covalently bonded compounds containing only hydrogen and carbon. The differences in their strucmral formulas are apparent the alkanes have only single bonds in their structural formulas, while the alkenes have one (and only one) double bond in their structural formulas. There are different numbers of hydrogen atoms in the two analogous series. This difference is due to the octet rule that carbon must satisfy. Since one pair of carbon atoms shares a double bond, this fact reduces the number of electrons the carbons need (collectively) by two, so there are two fewer hydrogen atoms in the alkene than in the corresponding alkane. 

There are two fewer hydrogen atoms in each of the alkenes than in the alkane with the same number of carbon atoms. This is also shown by the general molecular formula of the alkenes, C H2 , as opposed to the general molecular formula of the alkanes, which is C H2n+2-... 

Just as the alkanes and alkenes had general formulas, the carbon derivatives all have general formulas. The hydrocarbon backbone provides a portion of the general formula, and the functional group provides the other part. In each case, the hydrocarbon derivative is represented by the formula R-, and the hydrocarbon backbone has its own specific formula. The term substituted hydrocarbon is another name for hydrocarbon derivative, because the functional group is substituted for one or more hydrogen atoms in the chemical reaction. 

Thermal decomposition of LiR eliminates a /6-hydrogen atom to give an olefin and LiH, a process of industrial importance for long-chain terminal alkenes. Alkenes can also be produced by treatment of ethers, the organometallic reacting here as a very strong base (proton acceptor) ... 

A hydrogen atom is transferred from the metal to one of the alkene carbon atoms, forming a partially reduced intermediate with a C H bond and carbon-metal tr bond. 

This allylic bromination with NBS is analogous to the alkane halogenation reaction discussed in the previous section and occurs by a radical chain reaction pathway. As in alkane halogenation, Br- radical abstracts an allylic hydrogen atom of the alkene, thereby forming an allylic radical plus HBr. This allylic radical then reacts with Br2 to yield the product and a Br- radical, which cycles back... 

Treatment of an alkyl halide with a strong base such as KOH yields an. alkene. To find the products in a specific case, locate the hydrogen atoms on each carbon next to the leaving group. Then generate the potential alkene products by removing HX in as many ways as possible. The major product will be the one that has the most highly substituted double bond—in tints case, 1-methylcyclohexene. 

The difference in reactivity between the isomeric menthyl chlorides is due to the difference in their conformations. Neomenthyl chloride has the conformation shown in Figure 11.20a, with the methyl ancl isopropyl groups equatorial and the chlorine axial—a perfect geometry for L2 elimination. Loss of the hydrogen atom at C4 occurs easily to yield the more substituted alkene product, 3-menthene, as predicted by Zaitsev s rule. 

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