Pushing Electrons
4th Edition
ISBN: 9781133951889
Author: Weeks, Daniel P.
Publisher: Cengage Learning
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Complete the following heterocyclic reactions:
Out of SN1 and SN2, which reaction occurs with(a) Inversion of configuration(b) Racemisation
Please show the mechanism with arrow formalism.
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- Indane can undergo free-radical chlorination at any of the alkyl positions onthe aliphatic ring Draw the possible dichlorinated products from this reaction.arrow_forwardIndane can undergo free-radical chlorination at any of the alkyl positions onthe aliphatic ring.Draw the possible dichlorinated products from this reaction.arrow_forwardDraw an arrow pushing mechanism for this SN1 reactionarrow_forward
- Circle the most stable carbocation.arrow_forwardWrite the mechanism for the following reaction step using curvedarrows, and draw the result of those motions. You will need to draw adifferent conformation of the reactant.arrow_forwardDraw the product of syn addition of H2 across the double bond of the alkene in the drawing area below.arrow_forward
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