Triphenylcarbinol( or triphenylmethanol) gets its phenyl groups from phenylmagnesium bromide.
Synthesis of triphenylcarbinol:
A typical laboratory experiment for demonstrating the Grignard reaction is the synthesis of triphenylmethanol using methyl benzoate, benzophenone, and phenylmagnesium bromide. Diethyl carbonate is a possible starting material.
Characteristics:
- An organic substance is a triphenylmethanol. It is a white, crystalline substance that dissolves well in alcohol, diethyl ether, and benzene but not in water or petroleum ether. Due to the creation of a persistent "trityl" carbocation, it generates a bright yellow hue in very acidic solutions. Important dyes include several triphenylmethanol derivatives.
- Triphenylmethanol has a core tetrahedral carbon atom, three phenyls (Ph) rings, and an alcohol group attached to it. With lengths of around 1.47Å for all three C-Ph bonds and 1.42Å for the C-O link, these connections are characteristic of sp3-sp2 carbon-carbon bonds.
- Three neighboring phenyl groups give off specific qualities that are reflected in the alcohol's reactivity.
Learn more about triphenylmethanol here:
brainly.com/question/15089315
#SPJ4
Answer:
I don't think you can go on without doing a reaction since you touch really anything so no you can not go without any chemical reaction I think this is the answer
thats very nice lol, things stuck in amber are very cool
Answer:
the answeer is definitely silicon.
Answer:
Number of moles = 1.57 mol
Explanation:
Given data:
Mass of propanol = 94.1 g
Molar mass of propanol = 60.1 g/mol
Number of moles of propanol = ?
Solution:
Formula:
Number of moles = mass/molar mass
by putting values,
Number of moles = 94.1 g/ 60.1 g/mol
Number of moles = 1.57 mol
