Chemistery

                                          Wittig Reaction Wittig reaction turns a carbonyl ( compound that has C=O) to an alkene by reacting a carbonyl (aldehyde or ketone) with a phosphorus ylide . It is a very useful reaction that turns a C=O to a desired C=C. Making ylide Let's talk about the phosphorus ylide . It has no overall charge, but it has a negatively charged carbanion that is bonded to a positively charged phosphorus. It is prepared by a two-step reaction sequence - an SN2 in which a triphenylphosphine attacking an unhindered alkyl halide (making a positively charged phosphorus), followed by a proton abstraction by a strong base (usually butyllithium ). We know that Phosphorus and Sulfur can form more than 4 bonds using the d orbitals . One may think that the ylide should have a double bond instead of having the carbon and phosphorus ch...

Hoffman elimination and Cope elimination are amine chemistry. Both reactions are concerted and both favor the Hofmann product (less-substituted alkene). Hofmann Elimination  Leaving group  The general form of an amine is R-NH2. The amide ion is a strong base hence a poor leaving group. So if we want an amine to undergo an elimination, we have to make a better leaving group first. We do this by exhaustive methylation (usually with methyl iodide) to convert the leaving group into a quaternary ammonium salt which can leave as a neutral amine. E2 Mechanism Hofmann elimination follow a E2 , concerted reaction mechanism which needs a strong base . The geometry is specific here (like a typical E2): anti-coplanar between the proton being abstracted and the leaving group. The quaternary ammonium salt is reacted with silver oxide to become a hydroxide salt to generate the strong base needed. Heat is applied and the Hofmann product is the major product.  Hofmann Eli...

Dehydration of alcohols This is a reversible acid-catalyzed reaction. In fact, it is a common way to turn an alkene  into an alcohol. To increase the yield of the product, the alkene  produced is usually distilled off (an alkene has a lower boiling point than its alcohol due to the lack of hydrogen bonding) to shift the equilibrium to the product side. Concentrated sulfuric acid is used as a catalyst to protonate the -OH group to a better leaving group, H2O. Then, a E1 mechanism is followed: 1. ionization (water leaves) to a crabocation 2. a weak base (water or HSO4-) abstracts the proton to form an alkene.  Dehydration of alcohol Cracking (alkane) An industrial (large scale and least expensive) way to make alkene is by the catalytic cracking of alkane (e.g. petroleum). A long chain of alkane is heated with catalyst (e.g. platinum) to form small alkenes (around 6 carbon atoms). This process of dehydrogenation is endothermic, but it has a positive entropy change...

Alkene can be synthesized by a various ways. Alkene can be made from a carbonyl , alkyne , alkane , alchols , alkyl halide and vicinal dibromides and other elimination reactions. We will split the 7 methods of alkene  synthesis into 4 parts. Part 1: Alkyl halide and vicinal   dibromide Part 2: Alcohol,  alkyne  and alkane Part 3: Hofmann & Cope Elimination Part 4: Wittig Dehydrohalogenation of Alkyl halide  We already talk about how to synthesize alkene from a E2 (E1 is not considered because it often produces a mixture of SN1 and E1 products) reaction. Dehydrohalogenation of a alkyl halide is actually another name describing the same reaction we previously discussed in the E2 section. The alkyl halide loses a proton and a leaving group with a formation of an alkene . Remember that it is a stereospecific reaction (anti-coplanar) and the Zaitsev product is the major product (the opposite of a Zaitsev product is a Hofmann product, which i...