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- Which reaction below give a par of diastereomers and Why?please DRAW the full mechanism of the Na2S2O4 reduction reaction belowExplain the following result. Acetic acid (CH3COOH), labeled at its OH oxygen with theuncommon 18O isotope (shown in red), was treated with aqueous base, and then the solution was acidied. Two products having the 18O label at different locations were formed.
- Explain the following result. Acetic acid (CH3COOH), labeled at its OH oxygen with theuncommon 18O isotope (shown in red), was treated with aqueous base, and then the solution was acidified. Two products having the 18O label at different locations were formed.Account for the rapid rate of methanolysis of ClCH2OCH2CH3 even though the substrate is a primary halide. Hint: The reaction of the substrate with ethanol proceeds by SN1 mechanism. Draw the Lewisstructures.Explain the E2 mechanism (bimolecular elimination) of of Elimination ?
- One possible way of determining the identity of an alkene, is to let itundergo an oxidative cleavage reaction in the presence of hot basicpotassium permanganate. You are given two containers said to containdifferent alkenes. Container A is marked as cis / trans‐2‐butene andcontainer B as 2‐methyl‐1‐butene. Explain by referring to the formation ofproducts, how you would verify the identity of the alkenes.which newman projection displays the proper antiperiplanar orientation for an E2 elimination of the reaction sequence belowWhat is the curved arrow mechanism of t-butyl chloride treated with silver nitrate in ethanol (AgNO3 in EtOH)? Thank you for the help!
- Draw the curly arrow mechanism of the following reaction. [If possible, give 3 different ways to answer]A compound with the formula C8H12 absorbs two equivalents of H2 on Catalina reduction over a palladium catalyst to give compound A. Ozonalysis oxidative cleavage of the unknown compounds gives two compounds B and C.a. What alkene would give only a ketone with three carbons as a product of oxidative cleavage? b. What alkenes would give only an aldehyde with four carbons as a product of oxidative cleavage?