Custom eBook for Organic Chemistry
2nd Edition
ISBN: 9798214171104
Author: Straumanis
Publisher: Cengage Custom
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Chapter NW1, Problem 3E
Name each of the following structures.
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Part 4. Butanoic acid (ka= 1.52× 10-5) has a partition coefficient of 3.0 (favors benzene) when distributed bet.
water and benzene. What is the formal concentration of butanoic acid in each phase when
0.10M aqueous butanoic acid is extracted w❘ 25 mL of benzene
100 mL of
a) at pit 5.00
b) at pH 9.00
Calculate activation energy (Ea) from the following kinetic data: Temp (oC) Time (s) 23.0 180. 32.1 131 40.0 101 51.8 86.0 Group of answer choices 0.0269 kJ/mole 2610 kJ/mole 27.6 kJ/mole 0.215 kJ/mole 20.8 kJ/mole
Calculate activation energy (Ea) from the following kinetic data: Temp (oC) Time (s) 23.0 180. 32.1 131 40.0 101 51.8 86.0 choices: 0.0269 kJ/mole 2610 kJ/mole 27.6 kJ/mole 0.215 kJ/mole 20.8 kJ/mole
Chapter NW1 Solutions
Custom eBook for Organic Chemistry
Ch. NW1 - Prob. 1CTQCh. NW1 - (E) Write a correct name below each of the...Ch. NW1 - (E) What suffix do all the names in Model 1 have...Ch. NW1 - (E) What prefix stands for eight carbons?Ch. NW1 - Prob. 5CTQCh. NW1 - Prob. 6CTQCh. NW1 - Prob. 7CTQCh. NW1 - Prob. 8CTQCh. NW1 - Prob. 9CTQCh. NW1 - Use Model 1 to propose names for three-, four-,...
Ch. NW1 - Prob. 11CTQCh. NW1 - Prob. 12CTQCh. NW1 - Prob. 13CTQCh. NW1 - Name the following alkanes.Ch. NW1 - (Check your work.) Explain what is wrong with each...Ch. NW1 - Prob. 16CTQCh. NW1 - Draw the following alkanes a....Ch. NW1 - Prob. 18CTQCh. NW1 - Draw structures that correspond to the following...Ch. NW1 - For mono-substituted cycloalkanes the “1” is not...Ch. NW1 - Prob. 21CTQCh. NW1 - Prob. 22CTQCh. NW1 - Prob. 23CTQCh. NW1 - Prob. 24CTQCh. NW1 - Prob. 25CTQCh. NW1 - Write the name of the molecule on the left using...Ch. NW1 - Prob. 1ECh. NW1 - Prob. 2ECh. NW1 - Name each of the following structures.
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- Determine the rate law for sodium thiosulfate from the following data: [Na2S2O3] Time (s) 0.0318 230. 0.0636 57.5arrow_forwardPlease solvearrow_forwardRank the compounds in each group below according to their reactivity toward electrophilic aromatic substitution (most reactive = 1; least reactive = 3). Place the number corresponding to the compounds' relative reactivity in the blank below the compound. a. CH₂F CH3 F b. At what position, and on what ring, is bromination of phenyl benzoate expected to occur? Explain your answer. :0: C-O phenyl benzoate 6.Consider the reaction below to answer the following questions. A B C NO₂ FeBr3 + Br₂ D a. The nucleophile in the reaction is: BODADES b. The Lewis acid catalyst in the reaction is: C. This reaction proceeds d. Draw the structure of product D. (faster or slower) than benzene.arrow_forward
- Part 2. A solution of 6.00g of substance B in 100.0mL of aqueous solution is in equilibrium, at room temperature, wl a solution of B in diethyl ether (ethoxyethane) containing 25.0 g of B in 50.0 mL 9) what is the distribution coefficient of substance B b) what is the mass of B extracted by shaking 200 ml of an aqueous solution containing 10g of B with call at room temp): i) 100 mL of diethyl ether ii) 50ml of diethyl ether twice iii) 25ml of diethyl ether four timesarrow_forward- Rank the following groups of compounds from most acidic (1) to least acidic (4). Place the number corresponding to the compound's relative rank in the blank below the structure. a. NO₂ NO₂ CH2CH2CH2CH2OH CH3 CH3CH2CHOH CH3CH2CH2CH2OH NO₂ CH3CHCH2CH2OH b. OH OH CH₂OH CO₂H HC CN CN CNarrow_forwardGive the major organic product(s) of the following reactions or sequences of reactions. Show all relevant stereochemistry a. H MgBr 1. ether 2. H₂O* 4 COH b. 1. LIAIH, ether 2. H₂O Choose the best reagent(s) for carrying out the following conversions from the list provided below. Place the letter of the best choice in the blank to the left of the conversion. Reagents may be used more than once. a. 1. CH3MgBr, ether 2. H3O+ NaOH b. 1. PBr3 2. C. 2. 1. (CH3)3SiCl, (CH3CH2)3N CH3MgBr, ether 3. H₂O*+ 2. H3O+ e. 1. p-TosCl, pyridine f. نها g. 2. NaOH CrO3, H₂SO4, H₂O 1. NaBH4, ethanol 2. H30* h. PCC, CH2Cl2 Ovoldo-6 a. b. OH OH H OH O any organicarrow_forward
- Determine the rate law for sodium thiosulfate from the following data: [Na2S2O3] Time (s) 0.0318 230. 0.0636 57.5arrow_forwardDon't used hand raiting and don't used Ai solutionarrow_forwardDetermine the rate order from the following data: [Na2S2O3] Time (s) 0.0455 M 180.0 0.0909 M 90.0 0.136 M 60.0 Group of answer choices First order Second order Third order Zero orderarrow_forward
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