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- In a typical laboratory setting, a reaction is carried out in a ventilated hood with air circulation provided by outside air. A student noticed that a reaction that gave a high yield of a product in winter gave a low yield of that same product in the summer, eventhough his technique did not change and the reagents and co centrations used were identical. What is a plausible explanation for the different yield?If the rate constant in a first-order degradation reaction of a drug product is 0.462/year, what is the shelf-life of the drug product in months?The active ingredient in Benadryl Elixir is diphenhydramine hydrochloride, which slowly decomposes while on the shelf. The product should not be used if more than 10.% of the active ingredient has decomposed. If the product was prepared in November 2020 and the degradation process follows first-order kinetics with a half-life of 110 months, determine the expiration date that should be printed on the label of the product.
- 2,2-dimethylpropane only reacts with bromine in a solvent of CCl4. The presence of sunlight is required in this reaction. Specify the type of reaction and show the complete mechanism for the reaction occurred. This is a free radical halogenation, however I don't understand what it meant by "only recats with bromine in a solvent of CCL4"... can I have some explanation :(A scientist wants to look into the kinetics of the degradation of atrazine (A). There are 2 ways for degradation to occur. First, dealkylation to develop deisopropylatrazine (B) and deethylatrazine (C) with a kinetic constant of k1. Second, hydrolysis to create hydroxyatrazine (D) and N-isopropylammelide (E) with a kinetic constant k2. For all the mentioned species, derive their concentration profiles as a function of time when a batch reactor is utilized.Describe the reaction mechanism for the hydrolysis of 2-bromo-2-methylpropane [CH3C(CH3)2Br] with aqueous hydroxide ions (OH-).The description should be detailed and must include the type of bond fission that takes place. You may sketch and insert suitable diagrams to aid your description if you wish
- A2 Please write down the reaction mechanismThe active ingredient in Benadryl Elixir is diphenhydramine hydrochloride, which slowly decomposes while on the shelf. The product should not be used if more than 10.% of the active ingredient has decomposed. If the product was prepared in November 2020 and the degradation process follows first-order kinetics with a half-life of 110 months, determine the expiration date that should be printed on the label of the product. (Report the answer to the month and year.)An unknown inorganic phosphate undergoes first-order dehydration in a drying oven. Initially, the excess water content is measured to be 1.13 mg. After 2.10 days the water content is reduced to 0.488 mg. After 4.40 days, water content is only 0.194 mg. Determine the half-life of hydration under these conditions.
- 1. The rate constants for the formation of Co(NH 3 )5 X]^ 2+ from [Co(NH 3 )5 H 2 O]^ 3+ for X=Cl^ -; Br^ - , N 3 ^ - and SCN^ - differ by no more than a factor of two. Write out each step in the overall reaction and indicate the mechanism of substitution.The bromination of aceton is acid –catalyzed. CH3COCH3 + Br2 + H+ ---------> CH3COCH2Br + 2H+ + Br- The rate of disappearance of bromine was measured for several different concentrations of acetone, bromine, and H+ ion at a certain temperature. A B C [ CH3COCH3] [Br2] [ H+] Rate of disapperance [ Br2] 0.30 0.050 0.050 5.7 x 10 -5 0.30 0.10 0.050 5.7 x 10 –5 0.30 0.050 0.10 1.2 x 10 -4 0.40 0.050 0.20 3.1 x 10 -4 Write the rate law. Find the rate constant. Determine the half-life of the reaction if the [A]o = 0.50M ; [B]o = 0.40 M; [C]o = 0.6 M. ( Half-life is based on over all order of the reacaction)Optically pure Compound 1 undergoes a reaction at room temperature with sodium methoxide (NaOCH3) in methanol to form a single isomer of Compound 2 as shown below: 3. The rate of the above reaction is determined experimentally to follow second-order kinetics. Give a fully labelled sketch of a reaction coordinate diagram for the reaction. 4. draw a mechanism on a piece of paper (using curly arrows) to show the formation of Compound 2 from Compound 1 including any activated complex.