The reaction between ethyl iodide and hydroxide ion in ethanol (C2H5OH) solution,
C2H5OH) solution, C2H5I (alc)+OH-(alc)→C2H5OH(l)+I-(alc), has an activation energy of 86.8kJ/ mol and a frequency factor of 2.10X1011 M-1S-1. (a) Predict the rate constant for the reaction at 350C. (b) A solution of KOH in ethanol is made up by dissolving 0.335 g KOH in ethanol to form 250.0 ml of solution. Similarly, 1.453 g of C2H5I is dissolved in ethanol to form 250. ml of solution, Equal volumes of the two solutions are mixed. Assuming the reacting is first order in each reactant, what is the initial rate at 350C? (c) Which reagent in the reaction is limiting, assuming the reaction proceeds to completion? (d) Assuming the frequency factor and activation energy do not change as a function of temperature, calculate the rate constant for the reaction at 500C.
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Chapter 14 Solutions
Chemistry, The Central Science, Volume 1, Custom For Houston Community College
- Q1: For each molecule, assign each stereocenter as R or S. Circle the meso compounds. Label each compound as chiral or achiral. + CI OH woཡི།༠w Br H مه D CI ပ။ Br H, Br Br H₂N OMe R IN Ill N S H CI Br CI CI D OH H 1/111arrow_forwardDraw the two products of the reaction. H₂C. CH₂ H :0: CH3 CH₂ +1arrow_forwardShow work. Don't give Ai generated solutionarrow_forward
- ASP.....arrow_forwardQuestion 7 (10 points) Identify the carboxylic acid present in each of the following items and draw their structures: Food Vinegar Oranges Yogurt Sour Milk Pickles Acid Structure Paragraph ✓ BI UAE 0118 + v Task: 1. Identify the carboxylic acid 2. Provide Name 3. Draw structure 4. Take a picture of your table and insert Add a File Record Audio Record Video 11.arrow_forwardCheck the box under each structure in the table that is an enantiomer of the molecule shown below. If none of them are, check the none of the above box under the table. Molecule 1 Molecule 2 IZ IN Molecule 4 Molecule 5 ZI none of the above ☐ Molecule 3 Х IN www Molecule 6 NH Garrow_forward
- Highlight each chiral center in the following molecule. If there are none, then check the box under the drawing area. There are no chiral centers. Cl Cl Highlightarrow_forwardA student proposes the following two-step synthesis of an ether from an alcohol A: 1. strong base A 2. R Is the student's proposed synthesis likely to work? If you said the proposed synthesis would work, enter the chemical formula or common abbreviation for an appropriate strong base to use in Step 1: If you said the synthesis would work, draw the structure of an alcohol A, and the structure of the additional reagent R needed in Step 2, in the drawing area below. If there's more than one reasonable choice for a good reaction yield, you can draw any of them. ☐ Click and drag to start drawing a structure. Yes No ロ→ロ 0|0 G Х D : ☐ பarrow_forwardटे Predict the major products of this organic reaction. Be sure to use wedge and dash bonds when necessary, for example to distinguish between different major products. ☐ ☐ : ☐ + NaOH HO 2 Click and drag to start drawing a structure.arrow_forward
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