A certain reaction has the form aA → Products At a particular temperature, concentration versus time data were collected. A plot of 1/ [A] versus Lime (in seconds) gave a straight line with a slope of 6.90 × 10 −2 . What is the differential rate law for this reaction? What is the integrated rate law for this reaction? What is the value of the rate constant for this reaction? If [A] 0 for this reaction is 0.100 M, what is the first half-life (in seconds)? If the original concentration (at t = 0) is 0.100 M, what is the second half-life (in seconds)?
A certain reaction has the form aA → Products At a particular temperature, concentration versus time data were collected. A plot of 1/ [A] versus Lime (in seconds) gave a straight line with a slope of 6.90 × 10 −2 . What is the differential rate law for this reaction? What is the integrated rate law for this reaction? What is the value of the rate constant for this reaction? If [A] 0 for this reaction is 0.100 M, what is the first half-life (in seconds)? If the original concentration (at t = 0) is 0.100 M, what is the second half-life (in seconds)?
Solution Summary: The author explains the differential and integrated rate law, the rate constant, and the first and second half-life values for the given reaction.
At a particular temperature, concentration versus time data were collected. A plot of 1/ [A] versus Lime (in seconds) gave a straight line with a slope of 6.90 × 10−2. What is the differential rate law for this reaction? What is the integrated rate law for this reaction? What is the value of the rate constant for this reaction? If [A]0 for this reaction is 0.100 M, what is the first half-life (in seconds)? If the original concentration (at t = 0) is 0.100 M, what is the second half-life (in seconds)?
Kumada Coupling:
1. m-Diisobutylbenzene below could hypothetically be synthesized by Friedel-Crafts reaction. Write out the reaction with a
mechanism and give two reasons why you would NOT get the desired product.
Draw the reaction (NOT a mechanism) for a Kumada coupling to produce the molecule above from m-dichlorobenzene.
Calculate the theoretical yield for the reaction in question 2 using 1.5 g of p-dichlorobenzene and 3.0 mL isobutyl bromide.
What signals appeared/disappeared/shifted that indicate that you have your intended product and not starting material? What
other impurities are present in your product and how do you know?
Wintergreen from Aspirin:
1. In isolating the salicylic acid, why is it important to press out as much of the water as possible?
2. Write the mechanism of the esterification reaction you did.
3.
What characteristic absorption band changes would you expect in the IR spectrum on going from aspirin to salicyclic acid and
then to methyl salicylate as you did in the experiment today? Give approximate wavenumbers associated with each functional
group change.
What signals appeared/disappeared/shifted that indicate that you have your intended product and not starting material? What
other impurities are present in your product and how do you know?
Synthesis of ZybanⓇ:
1. Write a mechanism for the bromination of m-chloropropiophenone.
Br₂
CH2Cl2
Cl
Br
2. Give the expected m/z (to a round number) for the molecular ion from the product above (including isotopic peaks).
3. What signals appeared/disappeared/shifted that indicate that you have your intended product and not starting material? What
other impurities are present in your product and how do you know?
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