Select the resonance stabilised cation and give reason for your answer.
The resonance-stabilized cation is the allyl cation (C₃H₅⁺).
The reason for this is that the positive charge on the allyl _________ __________ ___ __________ _____ _____.
________ __________ ___ ___ _____ _____ _____ ______ __________ _________ _________ _________.
__________ __________ ______ __________ ______ _________ _____ _____ __________ ________.
____ _______ _____ _________ ______ __________ _____ ________ _____ _____ ______.
_____ __________ ____ ________ ___ __________ _________.
_______ ______ _______ _______ _____ _______ ________ _________ _________ ___ _______ __________.
_________ _____ ___ _________ _____ ______ __________ ___ ________ _____ ____.
___ _______ _________ _____ _________ __________ ___ __________ _________ _______.
________.
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Select the resonance stabilised cation and give reason for your answer.
Carry out the following conversions as indicated.
a) Fischer form to: i) Staggered and Eclipsed Sawhorse forms and
ii) Staggered and Eclipsed Newman forms
b) Flying wedge form to Fischer forms
Write the products formed in each of the following and give the mechanism.
Does a carbanion behave as an acid or a base? Explain the stability of carbanion on the basis of this behaviour?
Draw the meso isomers of the following compounds.
Give any two applications of ORD and CD.
List the properties of diastereomers. Indicate whether the following are enantiomers or diastereomers.
