Organic Chemistry 1 and
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(2026-2027)
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, HX Turns Double Bond into Addition of X at MarkovNikov position
HBr, ROOR Turns Double Bond into Addition of X at Anti-MarkovNikov position
H₃O⁺ Turns Double Bond into Addition of Alcohol at MarkovNikov position
1)Hg(OAc)₂, H₂O 2)NaBH₄ Turns Double Bond into Addition of Alcohol at MarkovNikov position
1)BH₃, THF 2)H₂O₂, NaOH Turns Double Bond into Addition of Alcohol at Anti-MarkovNikov position with
stereo-chemistry
H₂, Pt Reduces Double Bond to Single Bond
Br₂ Brominates both double bond positions
Br₂, H₂O Brominates Anti-MarkovNikov Position, and adds Alcohol at MarkovNikov Postion
(Opposite Stereo Chemistry)
1)RCO₃H 2)H₃O⁺ Adds Alcohol to both double bond positions (Opposite Stereo Chemistry)
KMnO₄, NaOH cold Adds Alcohol to both double bond positions (Same Stereo Chemistry)
1)OsO₄ 2)NaHSO₃, H₂O Adds Alcohol to both double bond positions (Same Stereo Chemistry)
1)O₃ 2)DMS Splits Molecule at Double Bond site and adds Oxygen to both openings
1)xs NaNH₂ 2)H₂O Makes two Possible products: One only puts halogen on MarkovNikov Position,
and other puts on halogen on each side of triple bond, completely reduces triple
bond
xs HX Puts two halogens on MarkovNikov Position, completely reduces triple bond
HX Puts Halogen at MarkovNikov Position, but only reduces bond a little bit
H₂SO₄, H₂O, HgSO₄ Adds Ketone at MarkovNikov Position