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What is the major product of the reaction given below ?
meso -2 ,3 -dichiorobutane + Nal (aq) →
  • a)
    c/s-2-butene
  • b)
    1,3-butadiene
  • c)
    trans-2-butene
  • d)
    1-butene
Correct answer is option 'C'. Can you explain this answer?
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What is the major product of the reaction given below ?meso -2 ,3 -dic...
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What is the major product of the reaction given below ?meso -2 ,3 -dic...
The major product of this reaction is meso-2,3-dichlorobutane undergoing a nucleophilic substitution reaction with sodium iodide (NaI) in aqueous solution (aq) to form meso-2-iodo-3-chlorobutane.

The reaction follows an SN2 mechanism, where the nucleophile (iodide ion) attacks the electrophilic carbon center (the carbon atom to which the two chlorine atoms are attached) and displaces one of the chlorine atoms as a leaving group. The resulting product has an iodine atom and a chlorine atom attached to adjacent carbon atoms.

The stereochemistry of the molecule remains unchanged as the reaction occurs at a meso compound, which has a plane of symmetry that separates the two halves of the molecule, making it optically inactive.
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What is the major product of the reaction given below ?meso -2 ,3 -dic...
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What is the major product of the reaction given below ?meso -2 ,3 -dichiorobutane + Nal (aq) →a)c/s-2-buteneb)1,3-butadienec)trans-2-butened)1-buteneCorrect answer is option 'C'. Can you explain this answer?
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