organic chemistry

posted by .

how do you increase the yield of triphenylmethanol in a grignard reaction?

  • organic chemistry -

    see below

Respond to this Question

First Name
School Subject
Your Answer

Similar Questions

  1. organic chemistry

    If, by mistake, a chemist used 100% ethanol rather than diethyl ether as the reaction solvent, would the Grignard synthesis still proceed as expected?
  2. organic chemistry

    Explain why Grignard reagent cannot be prepared from an organic halide that contains a hydroxyl (-OH), a carboxyl (-COOH), a thiol (-SH), or an amino (-NH2 or -NH) group.
  3. Organic Chemistry

    What is the structure of the magnesium salt that is created as a byproduct of the Grignard reaction: bromobenzene + mg = phenylmagnesium bromide phenylmagnesium bromide + benzophenone = triphenylmethanol
  4. Orgo

    this is a repost because i am really stuck What is the structure of the magnesium salt that is created as a byproduct of the Grignard reaction: bromobenzene + mg = phenylmagnesium bromide phenylmagnesium bromide + benzophenone = triphenylmethanol
  5. organic chemistry

    how do you increase the yield of triphenylmethanol in a grignard reaction?
  6. organic chemistry

    What is the product of reaction of triphenylmethanol heated up with 40% HI in glacial acetic acid and then treated with sodium bisulfite?
  7. Chemistry!

    What is theoretical yield when 15.6g of bromobenzene & 8.3g of methyl benzoate is used in a Grignard reaction.
  8. organic chem

    what are some chemical reasons that might have resulted in a lower yield of a product on a grignard reaction. Something related to grignards being very reactive and since its the limiting reagent, any reaction that destroys it will …
  9. organic chem

    I prepared triphenylmethanol by a grignard reaction. At the end you add petroleum ether to the mixture and heat it up. It stayed a liquid and got dark and oily but never solidified. What went wrong?
  10. organic chemistry

    Did a grignard experiment where we were supposed to form triphenylmethanol but something went wrong. When we heated up the mixture with the petroleum ether, it didn't solidify, it turned dark and oily. What went wrong?

More Similar Questions