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The reaction scheme goes as follows: H2PtCl6 CH3--(CH2)5--CH==CH2 <-----------------> CH3--(CH2)2--CH2--CH3 1-Octene NaBH4 Octane Ethanol 6M HCl (diluted) Givens: 120µL = 0.12mL of 1-Octene 50µL = 0.050mL of H2PtCl6 1mL of Ethanol 125µL = 0.125mL of NaBH4 100µL = 0.100mL of diluted 6M HCl -------------------- My attempt: I know that we have to convert what we have to moles (using mmols) 0.12mL of 1-Octene (using the density=0.72g/mL) = 0.76 mmol 50µL H2PtCl6 = 0.234 mmol 1mL Ethanol = 17.1 mmol 125µL NaBH4 = 3.54 mmol we can ignore the HCl because it's diluted, right? (also since we don't know the % of actual HCl dilution, so we can't use the molarity to get moles) Since we are going from 1-Octene to Octane, we have gained an extra H+ and lost a double bond. So essentially, the H2PtCl6 catalyst must have given off a H+ (since Pt metal targets alkenes). My dilemma is that I'm unsure on how to find the actual limiting reactant, and what information I should use. There's too much given; but from my introspection, we only need 1-Octene and the Pt catalyst,
Show all the steps in the mechanism for the following reaction, When benzene is mixed with deuterated sulfuric acid, deuterium is slowly incorporated onto the ring. Show the mechanism for this reaction and explain how this relates the sulfonation of ..
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