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safely, no.

And it's stupied.

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17y ago

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Is the Williamson ether synthesis of Phenacetin an oxidation reduction or neither?

The Williamson ether synthesis of Phenacetin is a substitution reaction to form an ether, so it is neither oxidation nor reduction. It involves the reaction of an alkyl halide with a phenol in the presence of a base to form the ether product.


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James Maxwell answer to this question is the ether that transported the light energy of the sun to the earth. Physicists disputed the existence of the ether. Maxwell was right. The ether is manifested by the "free space impedance" z=Wb/C = 375 Ohms, the ratio ofa magnetic charge (Wb Webers, volt second) and an electric (C) . The ether charge is related to Planck's Constant h=CWb= 2/3E-33. The light from the sun carries energy E=hf = zC^2f. The free space impedance transmits the energy from the sun to the earth in the ether. The Ether Constants are Wb=500 atto (E-18) Webers (volt seconds) and C=4/3 Atto Coulombs. Plancks Constant is h=CWb and z=Wb/C= 375 Ohms.


Where is it possible to learn about Williamson Ether Synthesis?

Williamson Ether Synthesis is a type of chemical reaction. If an individual is wanting to learn more about this chemical reaction, they may take college level courses in chemistry. Additionally, there are many books on chemistry which have information on Williamson Ether Synthesis.


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Is diethyl ether soluble in hexane?

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What is the pka value of ether?

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How do you explain the preparation of ether by williamson synthesis?

The Williamson ether synthesis is a reaction that converts alcohols (R-OH) into ethers (R-O-R). The first step in this reaction is forming the conjugate base of the alcohol (called an alcoxide) by reacting the alcohol with sodium metal. This reaction forms hydrogen gas (H 2 ) as a biproduct, so if you perform this reaction take caution to keep all flame sources away during sodium addition.  The alcoxide can then be added to a suitable alkyl halide (typically a primary halide) to form the ether via anSN2 mechanism.  Example: An example of the Williamson ether synthesis to make diethyl ether.  However there are certain limitations of Williamson synthesis of ether. In Williamson Synthesis the attack is done by alkoxide ion. Alkoxide ion behaves as the neuoclophile as well as the base. When it behaves as the neuclophile it causes substitution reaction to occur the formation of ether. When it behaves as the base it causes the the elimination reaction to occur. With the formation of alkenes. These two reaction going from primary to secandory to tertiary alkyl halides.possibility of elimination reaction goes on increasing with the formation of more amount of alkene and less amount of ether .


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yes you should be able to and get to meet him but if you have a back stage pass and the back stage passes can be free to and you dont have to win them i a compation ether