The data below was collected from three trials of the following reaction:               2ClO2 (aq) + 2OH- (aq) --> ClO3- (aq) + ClO2- (g) + H2O (l)   [ClO2]o (M) [OH-]o (M) Initial Rate (M/s) 1 0.0500 0.100   5.75 x 10-2 2 0.100   0.100   2.30 x 10-1 3 0.100   0.0500 1.15 x 10-1 a) What is the generic rate law for this reaction? b) What is the order for each reactant? What is the order for the overall reaction? c) What is the complete rate law for this reaction?

Using the mechanism below, what would be the appropriate equilibrium constant expression for the overall reaction? Step 1: H(aq) + H₂O2(aq) → H3O₂ (aq) Step 2: H3O₂ (aq) + Br (aq) → HOBr(aq) + H₂O(1) Step 3: HOBr(aq) + H*(aq) + Br (aq) ← → Br₂(aq) + H₂O(1) K= K= K = K= [Br₂] [H₂O]2 [H+]2[Br]2 [H₂O₂] [H+]2[Br]2 [H₂O₂] [Br₂] [Br₂] [H+][Br] [H₂O₂] [Br₂] [H+12[Br-12 [H₂O₂] fast slow fast

4. Explain why the rate of formation of 1-azidopropane is different depending on which halopropane (X = F, Cl, Br, I) is used. Explain which halopropane will react fastest? ~X X = F, Cl, Br, I NaN №3 1-azidopropane

Consid organic mechanism: 0 E 1 H Explanation Say tu :Ö: Does this mechanism describe an acid/base reaction? Note for advanced students: we mean only acid-base reactions in the Brønsted-Lowry sense. 2. Which reactants, if any, are acting as Brønsted-Lowry acids? Check Which reactants, if any, are acting as Brønsted-Lowry bases? If you said this mechanism does describe an acid-base reaction, draw the products of the reaction on the right-hand side above. X 2222 1 S Yes! Certainly not. Who knows? We need more information to decide. 200 C Click and drag to start drawing a structure. X 2023 McGraw Hill LLC. All Rights Reserved. Terms of Use Privacy Center | Accessibility 2 OFF olo 18 Ar

Which of the following changes would NOT affect the rate of the reaction of methanoic acid with bromine? HCOOH(aq) + Br₂(aq) image 2H* (aq) + 2Br (aq) + CO₂(g) O Using 100 mL of HCOOH and 100 mL of Br2 instead of 300 mL of each. O Using 0.10 M HCOOH in the reaction instead of 0.20 M HCOOH. Adding a catalyst to the reaction system. O Performing the reaction at 60°C instead of at 25°C.

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