"Bromination of alkenes stilbene tribromide" Essays and Research Papers

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    Experiments

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    EXPERIMENT 1: REACTIONS OF ENOLATE IONS WITH CARBONYL GROUPS Aims In this experiment we used two techniques for the reactions of enolate ions with carbonyl groups. One technique used was Doebner reaction and the other technique used was Claisen-Schmidt reaction. Therefore the aim of this experiment is to synthesize trans p-methoxycinnamic acid and to synthesize dibenzalacetone via an aldol condensation reaction between acetone and benzaldehyde. The products would be recrystallized using ethanol

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    Surname Centre No. Candidate No. Paper Reference(s) Initial(s) Paper Reference Signature 7 0 8 1 7081/01 0 1 Examiner’s use only London Examinations GCE Chemistry Ordinary Level Paper 1 Wednesday 12 January 2011 – Afternoon Time: 1 hour 15 minutes Materials required for examination Nil Items included with question papers Nil Team Leader’s use only Question Leave Number Blank 1 2 3 4 5 6 7 8 9 Instructions to Candidates In the boxes above‚ write your centre number

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    Iit Jee

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    Gaseous State Start Practice | Polymers Start Practice | | | "Do if you have Time" Chapters | Aldehyde Ketone Start Practice | Solutions Start Practice | Solid State Start Practice | Mole Concepts Start Practice | Alkanes‚ Alkenes and Alk... Start Practice | Surface Chemistry Start Practice | Nuclear Chemistry Start Practice | Purification Characteriz... Start Practice | Environmental Chemistry Start Practice | Electrochemistry Start Practice | | |

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    Isolation of Casein

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    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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    C. carbon. D. oxygen. 14. Which of the following is not a halogen element? A. Chlorine B. Bromine C. Fluorine D. Oxygen 15. All chemical compounds can be divided into two classes. These classes are A. hydrocarbons and alcohols. B. alkanes and alkenes. C. aliphatic and aromatic. D. inorganic and organic. 16. Acetic acid is a compound known as A. bleach. B. mouthwash. C. vinegar. D. ammonia. 17. A carbon compound that contains oxygen between two hydrocarbon groups is known as a/an A. ether. B

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    DETAILED LESSON PLAN IN ADVANCED CHEMISTRY IV- Euler LEARNING OBJECTIVES At the end of the lesson‚ students are expected to: Write the IUPAC name of certain alcohol compounds; SUBJECT MATTER Topic: Nomenclature of Carboxylic Acid References: General‚ Organic and Biochemistry by Denniston‚ Topping and Caret. Page 283-289. Fundamentals of General‚ Organic and Biochemistry by John R. Holum. Page 418-425. Materials: Ball and stick model of compounds Overhead projector Textbooks Pictures of certain

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    Design Analysis of Phenol

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    Phenol‚ also known as carbolic acid‚ is an aromatic organic compound with the molecular formula C6H5OH. It is a white crystalline solid that is volatile. The molecule consists of a phenyl group (-C6H5) bonded to a hydroxyl group (-OH). It is mildly acidic‚ but requires careful handling due to its propensity to cause chemical burns. Phenol was first extracted from coal tar‚ but today is produced on a large scale (about 7 billion kg/year) from petroleum. It is an important industrial commodity as a

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    Haloalkane

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    of haloalkanes Haloalkanes are named by adding prefix fluoro‚ chloro‚ bromo or iodo to the name of the corresponding alkanes. Physical properties of haloalkanes Haloalkanes have stronger intermolecules force compared to alkanes and alkenes. Melting and Boiling Points Name Formula Physical State Melting Point/°C Boiling Point/°C Fluoromethane CH3F Gas -142 -78 Chloromethane CH3Cl Gas -97 -24 Bromomethane CH3Br Gas -94 4 Iodomethane CH3I Liquid -67 42 Chloroethane CH3CH2

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    people do not know about. Most people don’t even know how to pronounce the name (it is pronounced pin-een). Alpha-Pinene isn’t restricted to cannabis only; it is found in many different plants. The chemical structure of Alpha-Pinene is simple. It is an alkene that also contains a four-membered ring. Alpha-Pinene is emitted by many different plants in the world. What Does Alpha-Pinene Smell Like? Alpha-Pinene gives plants that signature fresh smell we that people love so much. The smell is most often

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    Procedure: The addition of 4.0 mL cyclohexanol‚ 1.0 mL of 85% phosphoric acid‚ and one boiling chip‚ were all added to a 10 mL round bottom flask that would be attached to the end of an assembled simple distillation set up. A sand bath was placed atop a hot plate‚ and the simple distillation mechanism was lowered into the sand bath with the bottom most piece (the 10 mL round bottom flask) submerged about half way. The distillation process was completed after a sufficient amount of liquid distillate

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