structure and bonding in alkenes

Alkenes: Structure and Stability Degrees of unsaturation saturated hydrocarbon CnH2n+2 cycloalkane (1 ring) CnH2n alkene (1 p-bond) CnH2n alkyne (2 p-bonds) CnH2n-2 For each ring or p-bond, -2H from the formula of the saturated alkane Degrees of unsaturation: # of rings and/or p-bonds … Alkenes Bonding and Structure: • Carbons in the double bond of butene are sp2 hybridized. These form 4 sigma bonds (bonds formed along the direction of the bonding plane) with additional carbon and hydrogen atoms in a tetrahedral structure with bond angles of 109.5 degrees. 02/21/2019 5 Structure of Alkenes • Figure 4.1 According to the orbital overlap model, a double bond consists of one bond formed by overlap of sp2 hybrid orbitals and one bond formed by overlap of parallel 2p orbitals. They are referred to as 'unsaturated' hydrocarbons because they have a carbon=carbon C=C double bond and other atoms can add to them via simpleaddition reactions. Ethene or ethylene, H 2 C=CH 2, is the simplest alkene example. • Side on p-p orbital overlap creates a π-bond. Alkanes have the general formula C n H 2n+2. (Not allowed) The sigma bond has similar properties to those found in alkanes, while the pi bond is more reactive. Chapter 5: Structure and Preparation of Alkenes: Elimination Reactions Alkenes (olefins) are hydrocarbons that contain a carbon-carbon double bond and are said to be "unsaturated." Chime in new window Since a double bond is present and each carbon is attached to 3 atoms (2 H and 1 C), the geometry is trigonal planar. Conceptually, ethylene can be formed in the hybrid orbital model by the bonding of two sp2- Because the “leftover” (unhybridized) 2p orbital is a 2p z orbital, its axis is the z-axis, which is perpendicular to the plane containing the axes of the sp2 orbitals. • Rotating by 90°breaks the pi bond. Thus, all of the atoms bonded to the sp2 hybridized carbon lie in a plane. Alkenes are generally prepared through β elimination reactions, in which two atoms on adjacent carbon atoms are removed, resulting in the formation of a double bond. Structure of Alkanes. 4.4c); they are oriented at the maximum angular separation of 120°. Alkenes - 3 atoms and 1 double bond = trigonal planar. Their adjacent atoms are connected with sigma bonds and form tetrahedral centers around the carbon atoms. Carbon-Carbon double bond length is ~ 1.34 Å (single bonds in alkane The Structure of Alkenes. Two overlapping triangles are present since each carbon is the center of a planar triangle. 4.1 STRUCTURE AND BONDING IN ALKENES 125 Fig. alkenes are a series of hydrocarbon molecules (made of carbon and hydrogen atoms). The alkenes comprise a series of compounds that are composed of carbon and hydrogen atoms with at least one double bond in the carbon chain. The two carbons of a C=C double bond are sp 2-hybridized. Remember, the sp 2 hybridization occurs when the s orbital is mixed with two p orbitals and therefore, three orbitals are mixed, and the outcome is three hybrid orbitals which are called sp 2 hybrid orbitals. Preparations include the dehydration of alcohols, the dehydrohalogenation of alkyl halides, and the dehalogenation of alkanes. Alkenes contain a double bond that is composed of one sigma and one pi bond between two carbon atoms. • Angles around the carbons in the double bond are ~ 120º. Chapter 6. This group of compounds comprises a homologous series with a general molecular formula of C n H 2 n, where n equals any integer greater than one. For example, an alkane with 2 (n) carbon atoms, will have 6 (2n + 2) hydrogen atoms. As these bonds are all single bonds, there is free rotation around all connections. The carbon atoms in the double bond are sp 2 hybridized, forming a planar structure. Why do you think the bond strength of the C-H bond alkane, alkene, and alkyne follows the pattern shown below?
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