The following molecule cleanly yields a single product when treated with sodium ethoxide. Draw the structure of the product. Draw one or more chair conformations to clearly demonstrate why one product forms from this reaction. :Br: NaOEt, EtOH

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Q: Compound X is treated with Br, to yield meso-2,3-dibromobutane. Draw the structure of compound X.

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Q: Compound X is treated with Br2 to yield meso-2,3-dibromobutane. Draw the structure of compound X.

A: The compound X which is when treated with Br2 to yield meso-2,3-dibromobutane is trans-2-butene.

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Q: Arrange the following group  in order of increasing priority. Q) -OCH3 -CH(CH3)2 -B(CH2CH3)2 -H

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A: Answer :-  . *********************************

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Q: What products are formed from monochlorination of (R)-2-bromobutane at C1 and C4? Assign R and S…

A: The product formed from the monochlorination of (R)-2-bromobutane at C1 can be given as follows:

Q: Write the IUPAC name of   compound, showing stereochemistry where relevant.

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Q: Draw the structure of (Z)-3-methylhept-3-ene. Be sure the stereochemistry is drawn clearly.

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