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Epoxidation of Alkenes – Some of the most important reactions of alkenes involve oxidation. – When we speak of oxidation, we usually mean reactions that form carbon–oxygen bonds. (Halogens are oxidizing agents, and the addition of a halogen molecule across a double bond is formally an oxidation as well.) – …

Addition of Carbenes to Alkenes – Methylene (:CH2) is the simplest of the carbenes: uncharged, reactive intermediates that have a carbon atom with two bonds and two nonbonding electrons. – Like borane (BH3), methylene is a potent electrophile because it has an unfilled octet. – It adds to the electronrich …

Catalytic Hydrogenation of Alkenes – Although we have mentioned catalytic hydrogenation before, we now consider the mechanism and stereochemistry in more detail. – Hydrogenation of an alkene is formally a reduction, with H2 adding across the double bond to give an alkane. – The process usually requires a catalyst containing …

Formation of Halohydrin – A halohydrin is an alcohol with a halogen on the adjacent carbon atom. – In the presence of water, halogens add to alkenes to form halohydrins. – The electrophilic halogen adds to the alkene to give a halonium ion, which is also electrophilic. – Water acts …

Addition of Halogens to Alkenes – Addition of Halogens to Alkenes gives vicinal dihalides. (A) Mechanism of Halogen Addition – A halogen molecule (Br2, Cl2, or I2) is electrophilic; a nucleophile can react with a halogen, displacing a halide ion: – In this example, the nucleophile attacks the electrophilic nucleus …

Hydroboration of Alkenes – We have seen two methods for hydrating an alkene with Markovnikov orientation. – What if we need to convert an alkene to the anti-Markovnikov alcohol? – For example, the following transformation cannot be accomplished using the hydration procedures covered thus far. – Such an anti-Markovnikov hydration …

– Oxymercuration–demercuration of alkenes is another method for converting alkenes to alcohols with Markovnikov orientation. Hydration of alkenes by Oxymercuration–Demercuration – Many alkenes do not easily undergo hydration in aqueous acid. – Some alkenes are nearly insoluble in aqueous acid, and others undergo side reactions such as rearrangement, polymerization, or …

Hydration of Alkenes will be discussed by Addition of Water Addition of Water: Hydration of Alkenes – An alkene may react with water in the presence of a strongly acidic catalyst to form an alcohol. – Formally, this reaction is a hydration (the addition of water), with a hydrogen atom …

Alkyl halides as Solvents – Alkyl halides are used primarily as industrial and household solvents. – Carbon tetrachloride (CCl4) was once used for dry cleaning, spot removing, and other domestic cleaning. – Carbon tetrachloride is toxic and carcinogenic (causes cancer), however, so dry cleaners now use 1,1,1-trichloroethane and other solvents …

Online MCQ test on Chemical Bonding – Lewis Theory – In this topic we offer you, online MCQ test in the fundmental of Chemical Bonding – Lewis Theory . – It is a simple test to measure the strength of your knowledge in the basics of understanding the topics of …

Addition of Hydrogen Halides to Alkenes : Markovnikov’s Rule Orientation of Addition: Markovnikov’s Rule – The simple mechanism shown for addition of HBr to but-2-ene applies to a large number of electrophilic additions. – We can use this mechanism to predict the outcome of some fairly complicated reactions. – For …

Electrophilic Addition to Alkenes Reactivity of the Carbon–Carbon Double Bond – All alkenes have a common feature: a carbon–carbon double bond. – The reactions of alkenes arise from the reactivity of the carbon–carbon double bond. – Once again, the concept of the functional group helps to organize and simplify the …

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Methods for Synthesis of Alkenes – Six methods for Synthesis of Alkenes will be discussed as follow: (1) Dehydrohalogenation of alkyl halides – Dehydrohalogenation is the elimination of a hydrogen and a halogen from an alkyl halide to form an alkene. – dehydrohalogenation can take place by the E1 and …

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