Version 1 2. undergoes a nucleophilic substitution reaction with HO- 2-Methyl-2-bromopropane ions in aqueous solution. B

Business, Finance, Economics, Accounting, Operations Management, Computer Science, Electrical Engineering, Mechanical Engineering, Civil Engineering, Chemical Engineering, Algebra, Precalculus, Statistics and Probabilty, Advanced Math, Physics, Chemistry, Biology, Nursing, Psychology, Certifications, Tests, Prep, and more.
Post Reply
answerhappygod
Site Admin
Posts: 899603
Joined: Mon Aug 02, 2021 8:13 am

Version 1 2. undergoes a nucleophilic substitution reaction with HO- 2-Methyl-2-bromopropane ions in aqueous solution. B

Post by answerhappygod »

Version 1 2 Undergoes A Nucleophilic Substitution Reaction With Ho 2 Methyl 2 Bromopropane Ions In Aqueous Solution B 1
Version 1 2 Undergoes A Nucleophilic Substitution Reaction With Ho 2 Methyl 2 Bromopropane Ions In Aqueous Solution B 1 (102.68 KiB) Viewed 51 times
Version 1 2. undergoes a nucleophilic substitution reaction with HO- 2-Methyl-2-bromopropane ions in aqueous solution. Br + HO™ (a) Complete the reaction equation, showing the structure of the organic product molecule. Name this product. [2%] (b) For the above reaction the following kinetics data were obtained: [C4H9Br] /mol dm-3 [HO] /mol dm-³ Reaction rate/mol dm-³ s-¹ 0.1 0.1 1 x 10-³ 0.3 0.1 3 x 10-³ 0.3 0.3 3 x 10-³ Using this information, write an expression for the rate of reaction with respect to the concentration of the relevant reagent(s). [3%] (c) The rate constant for this reaction at 55 °C is k = 0.01 s¹. Determine the half- life of C4H9Br in the reaction mixture. [2%] (d) Draw, using curly arrows, the mechanism for this reaction and identify the rate determining step. [5%] (e) The product of this reaction, C4H₂OH, burns in excess oxygen according to the reaction: C4H₂OH(1) + 6 O2 (g) 4 CO2(g) + 5 H₂O(g) Answer ALL parts (a) to (g).
Join a community of subject matter experts. Register for FREE to view solutions, replies, and use search function. Request answer by replying!
Post Reply