[Chemistry Class Notes] on Chemical Properties of Alkenes Pdf for Exam

In organic chemistry, we study the various types of compounds formed from the carbon atom. Based on its bonding organic compounds are of three types Alkanes (single bond), Alkenes (double bonds), and Alkynes (triple bonds). When there is a single bond between the carbon-carbon atom then it forms alkanes (C-C). Whenever there is a double bond between the carbon-carbon atom then alkenes (C=C) are formed. In case if it shares a triple bond between carbon-carbon atom then it is alkynes (C≡C). A large number of pi bonds are present in alkanes that are closely held due to which they show a variety of chemical properties.

Chemical Property of Alkenes

Single bond > Double bond >Triple bond

• Alkenes exist in all three solid-liquid and gaseous states.

• Alkenes are less soluble in water due to weak Van-Der-Waal forces

• The boiling point of alkenes depends on the molecular structure, the longer the molecular chain, the higher will be its boiling point.

• Functional groups are responsible for the polarity of alkenes.

Reactions of Alkenes

Another significant chemical property of alkene compounds which, in the addition of ozone or three molecules, led to the formation of ozone at which upon reduction with zinc dust and water produces aldehydes and ketones respectively. This reaction is also considered a method of preparation for aldehydes and ketones.

Oxidation reaction and Ozonolysis are prominently exhibited in the chemical properties of alkenes.

Reactions

Alkenes are less stable than alkanes, but they are more reactive. The majority of alkene reactions involve additions to this pi bond, resulting in the formation of new single bonds. Because alkenes may engage in a wide range of processes, including polymerization and alkylation, they are used as feedstock in the petrochemical industry.

With the exception of ethylene, alkenes have two reactivity sites: the carbon-carbon pi-bond and the presence of allylic CH centres. The former predominates, while the allylic site is also significant.

Many additional reactions occur in alkenes, which occur by opening up the double-bond. The majority of these addition reactions follow the electrophilic addition mechanism. Hydrohalogenation, halogenation, halohydrin production, oxymercuration, hydroboration, dichlorocarbene addition, the Simmons–Smith reaction, catalytic hydrogenation, epoxidation, radical polymerization, and hydroxylation are some examples.

The equivalent alkanes are produced through the hydrogenation of alkenes. The reaction is sometimes performed under pressure and at high temperatures. Almost often, metallic catalysts are necessary. Platinum, nickel, and palladium are the most common metals used in industrial catalysts. The manufacture of margarine is a large-scale application.

Many more H-can X’s can be added in addition to the insertion of H-H across the double bond. These procedures are frequently of significant commercial importance. The addition of H-SiR3, or hydrosilylation, is one example. This process produces organosilicon compounds. Another reaction is hydrocyanation, which occurs when H-CN is added across a double bond.

Alcohols are produced through hydration, which is the addition of water across the double bond of alkenes. Phosphoric acid or sulfuric acid catalyses the process. This process is carried out on a large scale in order to manufacture synthetic ethanol.

CH₂ = CH₂ + H₂O → CH₃ – CH₂OH

Alkenes can also be transformed to alcohol by the oxymercuration–demercuration reaction, the hydroboration–oxidation reaction, or Mukaiyama hydration.

The addition of elemental bromine or chlorine to alkenes results in vicinal dibromo- and dichloro alkanes (1,2-dihalides or ethylene dihalides) in electrophilic halogenation. The decolourization of a bromine solution in water is used to detect the presence of alkenes:

CH₂ = CH₂ + Br₂ →  BrCH₂ – CH₂Br

Related processes are also used to calculate the bromine and iodine numbers of a chemical or mixture as quantitative measurements of unsaturation.

The addition of hydrogen halides, such as HCl or HI, to alkenes, produces the equivalent haloalkanes:

CH₃ – CH = CH₂ + HI → CH₃ – CHI – CH₂ – H

If the two carbon atoms at the double bond are attached to a differing number of hydrogen atoms, the halogen preferentially occurs at the carbon with fewer hydrogen substituents. This pattern is referred to as Markovnikov’s rule. The employment of radical initiators or other chemicals might result in the opposite product outcome. In the presence of different contaminants or even ambient oxygen, hydrobromic acid, in particular, is prone to generating radicals, resulting in a reversal of the Markovnikov result: 

CH₃ – CH = CH₂ + HBr → CH₃ – CH – CH₂ – Br

Polymerization techniques use terminal alkenes as precursors to polymers. Some polymerizations are economically significant because they produce polymers polyethene and polypropylene. Although they contain no olefins, polymers derived from alkene are commonly referred to as polyolefins. Polymerization can occur through a variety of methods. Natural rubber is produced by conjugated dienes such as buta-1,3-diene and isoprene (2-methylbuta-1,3-diene).

Bonding and structure

A carbon-carbon double bond is made up of two bonds: a sigma bond and a pi bond. This double bond is stronger than a single covalent bond (611 kJ/mol for C=C vs. 347 kJ/mol for C–C), but it is not twice as strong. The average bond length of a double bond is 1.33 (133 pm) compared to 1.53 for a normal C-C single bond.

Each carbon atom in the double bond forms sigma bonds with three additional atoms by using its three sp2 hybrid orbitals (the other carbon atom and two hydrogen atoms). The pi bond is formed by the unhybridized 2p atomic orbitals that lie perpendicular to the plane formed by the axes of the three sp2 hybrid orbitals. This bond is located outside of the main C–C axis, with half of it on one side of the molecule and the other on the other. The pi bond is substantially weaker than the sigma bond, with a strength of 65 kcal/mol.

Because breaking the alignment of the p orbitals on the two carbon atoms incurs an energy penalty, rotation about the carbon-carbon double bond is limited. As a result, cis and trans isomers interconvert so slowly that they may be handled freely at room temperature without isomerization. 

For compounds with three or four distinct substituents, more complicated alkenes may be denoted using the E–Z notation (side groups). For example, in (Z)-but-2-ene (a.k.a. cis-2-butene), the two methyl groups occur on the same side of the double bond, but in (E)-but-2-ene (a.k.a. trans-2-butene), the methyl groups appear on opposing sides. Butene’s two isomers have differing characteristics.

The molecular geometry of alkenes contains bond angles of around 120° around each carbon atom in a double bond, as predicted by the VSEPR model of electron pair repulsion. The angle may change due to steric strain caused by nonbonded interactions between functional groups linked to the double bond’s carbon atoms. Propylene, for example, has a C–C–C bond angle of 123.9°.

Bredt’s rule asserts that a double bond cannot develop at the bridgehead of a bridged ring system unless the rings are sufficiently massive.

Using Fawcett’s definition of S as the total number of non-bridgehead atoms in the rings, bicyclic systems need S ≥7 while tricyclic systems require S ≥ 11.

Physical characteristics

Alkenes and alkanes have many physical features, such as being colourless, nonpolar, and flammable. The physical state is determined by molecular mass: the simplest alkenes (ethylene, propylene, and butene), like the equivalent saturated hydrocarbons, are gases at room temperature. Higher alkenes are waxy solids, while linear alkenes with five to sixteen carbon atoms are liquids. The melting point of solids rises with increasing molecular mass.

Alkenes have stronger odours than their comparable alkanes. The odour of ethylene is pleasant and musty. Cupric ion binding to olefin in the human olfactory receptor MOR244-3 is involved in the smell of alkenes (as well as thiols). Strained alkenes, in particular, norbornene and trans-cyclooctene, have strong, disagreeable scents, which is consistent with the stronger complexes they form with metal ions such as copper.

Focus on the features of alkenes and find out how they are unique from the rest. Learn how they form a family of compounds by showing similar reactions and other chemical properties.