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Steric hinderance between the ortho hydrogens makes it impossible for the three phenyl rings to be coplanar. Instead the triphenylmethyl.

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Presentation on theme: "Steric hinderance between the ortho hydrogens makes it impossible for the three phenyl rings to be coplanar. Instead the triphenylmethyl."— Presentation transcript:

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11 Steric hinderance between the ortho hydrogens makes it impossible for the three phenyl rings to be coplanar. Instead the triphenylmethyl carbocation assumes a “ propeller ” conformation with the phenyl rings pitched at a 32° angle.

12 The triphenylmethyl cation can be prepared by reaction of a Grignard reagent with benzophenone to form triphenylmethyl alcohol. Treatment with fluoboric acid results in the trityl carbocation.

13 Safety Notes for Expt. 30 – Synthesis of Triphenylmethanol and the Trityl Carbocation

14 Physical Properties of the Reactants and Reagents in Expt. 30

15 IR Spectra of bromobenzene and benzophenone

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18 Setup of the round-bottom flask, Claisen adapter, West condenser and addition funnel

19 A drying tube is added to the top of the condenser

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