Experiment 1: Isolation of Casein from Milk * pH of milk – 6.6 * milk = 87.1% water‚ 4.9 % CHO 3.9 %‚ fats‚ 0.7% minerals Experiment 2: Protein Hydrolysis and Characterization | Reagents | Principle | Test for | Positive Result | Negative Result | Biuret | CuSO4‚ NaOH | Complexation of Cu+2 with amide N atoms | Polypeptide bonds | Violet/purple solution | Blue color solution | Sakaguchi | 10% NaOH‚ 0.02% α-naphtol solution‚ 2% NaOBr | arginine condenses with α-naphtol and NaOH
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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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Introduction: For this lab‚ the main focused involved alkanes and hydrocarbons. Essentially‚ the free-radical chain of chlorination of 1-Chlorobutne. Free radical-chains occur because alkanes are chemically unreactive with most agents. However‚ the free-radical chain allows a pathway of certain functional groups like alkyl chloride or bromides. In addition‚ chlorine atoms can possibly be made from molecular chlorine under low to mild conditions with the usage of a catalytic amount of an initiator
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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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Organic Chemistry Experiment - Hydrocarbons Thursday‚ April 12‚ 2007 1:34 PM Purpose: To Identify an unknown Hydrocarbon Procedure: Procedure listed in handout "Organic Chemistry Experiment -- Hydrocarbons" Hazards: Open flame and hydrocarbons are flammable. Equations: 1. . 3. . 4. . 5. . Unknown #: 1B s-6 Hyd-3 (colorless liquid) Data/Observations: Test Bromine addition Alkane Mixture of hexane and dichloromethane was originally clear liquid. After adding 3 drops red color Br2/CH2Cl
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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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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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Lab 1: Alkene Addition: Bromination of (E)-stilbene I. Introduction: 1. The purpose of the experiment was to perform an electrophilic addition reaction by using pyridinium tribromide to brominate (E)-stilbene and to identify whether it formed the meso- or racemic product through melting point analysis. 2. This is the mechanism for the bromination of (E)-stilbene. However‚ this is the mechanism for Br2 and in class we us Pyridinium Tribromide instead due to the difficulties associated
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