1. The formation of molecular bromine (Br2) from HBr and KBrO3 must be derived using redox reactions. a. Write the balanced (ionic) redox equation for the conversion of BrO3 into Br2 under acidic conditions. Label the half reaction as either oxidation or reduction. 10e + 2Br03 + 12H* → Br₂ + 6H₂O (Reduction) b. Write the balanced (ionic) redox equation for the conversion of Br into Br2 under acidic conditions. Label the half reaction as either oxidation or reduction. 2Br → Br₂ + 2e¯ (Oxidation) C. Write the balanced net (ionic) redox reaction (reduced to the lowest whole number coefficients) 6H + BrO3 + 5Br¯ → 3Br2 + 3H20 d. Rewrite the balanced net redox equation in complete (molecular) form using KBrO3, HBr and CH3COOH as the reactants. (note that this step may require a bit of manipulation as there are two sources of H+ HBr and CH3COOH) KBгO3 + CH3COOH + 5HBr → 3Br2 + 3H2O + CH3COOK 2. Write the equation for the reaction of acetanilide with molecular bromine (for the organic compounds, draw the full structures, not condensed formulae). уго -Z are tanilide Br. Febrz H Во 4 P-bromo acetanilide
1. The formation of molecular bromine (Br2) from HBr and KBrO3 must be derived using redox reactions. a. Write the balanced (ionic) redox equation for the conversion of BrO3 into Br2 under acidic conditions. Label the half reaction as either oxidation or reduction. 10e + 2Br03 + 12H* → Br₂ + 6H₂O (Reduction) b. Write the balanced (ionic) redox equation for the conversion of Br into Br2 under acidic conditions. Label the half reaction as either oxidation or reduction. 2Br → Br₂ + 2e¯ (Oxidation) C. Write the balanced net (ionic) redox reaction (reduced to the lowest whole number coefficients) 6H + BrO3 + 5Br¯ → 3Br2 + 3H20 d. Rewrite the balanced net redox equation in complete (molecular) form using KBrO3, HBr and CH3COOH as the reactants. (note that this step may require a bit of manipulation as there are two sources of H+ HBr and CH3COOH) KBгO3 + CH3COOH + 5HBr → 3Br2 + 3H2O + CH3COOK 2. Write the equation for the reaction of acetanilide with molecular bromine (for the organic compounds, draw the full structures, not condensed formulae). уго -Z are tanilide Br. Febrz H Во 4 P-bromo acetanilide
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
Related questions
Question
Expert Solution
This question has been solved!
Explore an expertly crafted, step-by-step solution for a thorough understanding of key concepts.
Step by step
Solved in 1 steps with 2 images
Recommended textbooks for you
Chemistry
Chemistry
ISBN:
9781305957404
Author:
Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:
Cengage Learning
Chemistry
Chemistry
ISBN:
9781259911156
Author:
Raymond Chang Dr., Jason Overby Professor
Publisher:
McGraw-Hill Education
Principles of Instrumental Analysis
Chemistry
ISBN:
9781305577213
Author:
Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:
Cengage Learning
Chemistry
Chemistry
ISBN:
9781305957404
Author:
Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:
Cengage Learning
Chemistry
Chemistry
ISBN:
9781259911156
Author:
Raymond Chang Dr., Jason Overby Professor
Publisher:
McGraw-Hill Education
Principles of Instrumental Analysis
Chemistry
ISBN:
9781305577213
Author:
Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:
Cengage Learning
Organic Chemistry
Chemistry
ISBN:
9780078021558
Author:
Janice Gorzynski Smith Dr.
Publisher:
McGraw-Hill Education
Chemistry: Principles and Reactions
Chemistry
ISBN:
9781305079373
Author:
William L. Masterton, Cecile N. Hurley
Publisher:
Cengage Learning
Elementary Principles of Chemical Processes, Bind…
Chemistry
ISBN:
9781118431221
Author:
Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:
WILEY