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Solve this organic transformation....use - Br2,CCl4,KOH,CH3OH,Hg+2,diluted H2SO4, PCC,HBr,Mg,Dry ether,Na,H2,Pd,quinoline

Solve This Organic Transformationuse Br2CCl4KOHCH3OHHg2diluted H2SO4 PCCHBrMgDry EtherNaH2Pdquinoline class=

Sagot :

Organic transformation sequential equation using catalysts will be as follows:

2CH3-CH2-O => (alc. KOH) => CH2=CH2 + KCl + H2O => (Br2/CCl4) => CH2Br-CH2Br + Zn

CH2Br-CH2Br + Zn => (HBr /Pd) => CH2=CH2+ZnBr2

As can be visualized from above organic transformation equation, conversion of dry ether in presence of alkaline potassium hydroxide results in formation of unstable ethene. This dry unsaturated compound of ethene is stabilized by reaction that happens in presence of bromine or calcium tetrachloride as the catalyst which results in formation of ethylene bromide which in presence of highly efficient palladium as catalyst results in formation of stable ethene as byproduct. Thereby with formation of stable compound of ethylene, it releases zinc bromide as byproduct resulting completion of reaction equation. This stable product ethene is a double bonded carbon structure that is chemically extremely flammable and has planar structure.

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