1. Which of the following are the products of a homolytic cleavage of a C-C bond of ethane? A) 2 B) CH3 CH3 C) H D) 2 + + CH3 CH2H3 CH3 Ans: A Chapter 11 Topic: Radicals Section: 11.1 Difficulty Level: Easy 2. Which of the following is the most stable radical? A) B) C) D) E) Ans: B Chapter 11 Topic: Radicals Section: 11.1 Difficulty Level: Easy 3. In the molecule shown below‚ determine which of the labeled bonds is
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1. List all Functional Groups 2. What is an alkane? List its properties. 3. Write the name and formula of simple alkanes 4. Consider this compound (CH3)2CHCH2C(CH3)3. Name this. a. redraw it clearing all brackets and parentheses. b. Find the longest chain. Check from all directions. If it is not horizontal‚ rewrite the compound that so that longest chain IS horizontal. c. Number the carbons of the longest chain backwards and forwards.
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substituted benzenes towards bromination will be determined‚ where bromine is dissolved in acetic acid. Materials and apparatus Test solutions: 0.2 M solutions in ethyl acetate: Benzene‚ chlorobenzene‚ phenol‚ nitrophenol‚ aniline and acetanilide. Measuring pipettes (5 mL) micro test tubes 0.05 M Br2 in 90% CH3COOH Pasteur pipettes 0.05 M Br2 in cyclohexane II. Schematic Diagram of the Procedure Relative Rates of Bromination Add 2 drops of 0.05 M
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Exam Name___________________________________ MULTIPLE CHOICE. Choose the one alternative that best completes the statement or answers the question. 1) 1) Disregarding stereoisomers‚ how many different enols can the β-diketone CH3 COCH 2 COCH 2 CH3 form? A) 3 B) 1 C) 4 D) 0 E) 2 2) Methylamine reacts with acetophenone to yield the: A) imine. B) enamine. C) acetal. D) amide
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DIFFERENT REACTION WILL YIELDS TO A CONCLUSION OF WHAT IS/ARE THE FACTOR/S OF ELECTROPHILIC SUBSTITUTION ON AN ORGANIC COMPOUND – AROMATIC COMPOUNDS. There are three experiments in this chapter of the laboratory. First is the substitution by bromination. Second is the solvent effect which is dealing in the nature of the solvent. And third is the temperature test. Having this division in the experiment one‚ we can now conclude that substituent in substitution‚ the nature of the solvent polar or
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ranged from about 77 degrees in fraction 1 to about 89 degrees in the fraction 10. Next‚ the toluene stayed relatively the same temperature throughout the first 6 fractions at around 69 degrees and then drastically shot up to 100 degrees by the end of fraction 10. This is due to hexane having a lower boiling point and being able to steadily increase through each fraction evenly as temperature rises while the toluene‚ because of its higher boiling component‚ needed the higher temperature in order for higher
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Experiment 1: Bromination of Acetanilide1 Precautions: Ethanol is flammable Sodium hypochlorite is an oxidizing agent and releases toxic fumes (handle in fume hood) Acetic acid is corrosive‚ harmful if inhaled‚ flammable and can cause burns (handle in fume hood) Gloves are recommended to avoid chemical contact with skin Reaction Scheme: Conversion of acetanilide to p-bromoacetanilide Procedure: To a 125 mL Erlenmeyer flask containing a mixture of 95% ethanol (6 mL) and acetic acid (5 mL)‚ dissolve
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ºC) and toluene (bp 110.6 ºC). Analysis via gas chromatography allowed us to determine the relative percentage of hexane and toluene at fractions near the beginning and end of our distillations. Relative percentages have been recorded in the table below‚ and our calculations are shown on page 5. Simple Distillation Retention time (s) Fractional Distillation Retention time (s) Cyclohexane Retention time (s) Toluene Retention time (s) Cyclohexane Retention time (s) Toluene Retention
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three different eluents‚ hexane‚ toluene‚ and acetone. The chromatography compared aniline‚ 2‚ 4-dinitrobromobenzene‚ and a sample from the mixture of the two reactants when the reaction first began to take place. Another thin layer chromatography used a product sample an hour after the reaction first began and the eluent that showed the best separation of molecules. Table of Rf Values Table of Rf Values | Aniline | Product | 2‚ 4-Dinitrobromobenzene | Toluene | 0.083 | 0.104 | 0.333 | 0.583
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Iodine Crystal Solvents: Distilled water Ethyl Alcohol Toluene Solutions Polar‚ Non-Polar or Ionic Attractive Forces NaCl + Distilled Water Solute NaCl Solute-solute Solute-solvent Solvent Distilled water Solvent-solvent NaCl + Ethyl Alcohol Solute NaCl Solute-solute Solute-solvent Solvent Ethyl Alcohol Solvent-solvent NaCl + Toluene Solute NaCl Solute-solute Solute-solvent Solvent Toluene Solvent-solvent Naphthalene + Distilled Water Solute Naphthalene
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