How do triphenylphosphine and borane form a Lewis acid-base adduct? (a) The phosphorus atom in triphenylphosphine is less electronegative than the boron atom in borane and is thus attracted to boron to form the bond. (b) The phosphorus in triphenylphosphine exchanges with the boron from borane. (c) Triphenylphosphine donates the lone pair on its phosphorus to the electron-deficient boron in borane. (d) Triphenylphosphine donates a phenyl ring from its phosphorus to the electron-deficient boron in borane. (e) The phosphorus in triphenylphosphine accepts a proton from the proton-rich borane.

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Chapter1: Chemical Foundations
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How do triphenylphosphine and borane form a Lewis acid-base
adduct?
(a) The phosphorus atom in triphenylphosphine is less
electronegative than the boron atom in borane and is thus
attracted to boron to form the bond.
(b) The phosphorus in triphenylphosphine exchanges with the
boron from borane.
(c) Triphenylphosphine donates the lone pair on its phosphorus
to the electron-deficient boron in borane.
(d) Triphenylphosphine donates a phenyl ring from its
phosphorus to the electron-deficient boron in borane.
(e) The phosphorus in triphenylphosphine accepts a proton from
the proton-rich borane.
Transcribed Image Text:How do triphenylphosphine and borane form a Lewis acid-base adduct? (a) The phosphorus atom in triphenylphosphine is less electronegative than the boron atom in borane and is thus attracted to boron to form the bond. (b) The phosphorus in triphenylphosphine exchanges with the boron from borane. (c) Triphenylphosphine donates the lone pair on its phosphorus to the electron-deficient boron in borane. (d) Triphenylphosphine donates a phenyl ring from its phosphorus to the electron-deficient boron in borane. (e) The phosphorus in triphenylphosphine accepts a proton from the proton-rich borane.
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