Synthesis of p-Nitroacetanilide (electrophilic aromatic substitution) In this experiment‚ we convert acetanilide to p-nitroacetanilide. [pic] The mechanism for the nitration is that of electrophilic aromatic substitution. The nitronium ion is directed to the positions ortho and para to the acetamido (-NHCOCH3) group. This occurs because the resonance electron-releasing effect of that group increases the electron density at those positions‚ helping to stabilize the intermediates that
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BroIn this experiment of the relative rates of free-radical chain bromination‚ we were expected to be able to determine the relative reactivates of the many types of hydrogen atoms involved toward bromine atoms. Bromination is defined to be a regioselective reaction meaning bromine has preference of making or breaking a bond over all other directions that it may have had available. In this case‚ Markovnikov’s rule is revealed to be the case in this situation that states that adding a protic acid
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Purifying Acetanilide by Recrystallization Results: Acetanillide Solubility of acetanilide in water is 5.5g/100mL at 100C 0.53g/100mL at 0C PERCENT YIELD/THEORETICAL YIELD: Discussion: Acenatilide is a synthetic organic compound introduced in therapy in 1866 as a fever-reducing drug. Its effectiveness in relieving pain was discovered soon thereafter‚ and it was used as an alternative to aspirin. The solvent that I selected to recrystallize the
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LAB REPORT! EXPERIMENT#5‚6! MANPREET KAUR KHAIRA! LAB PARTNER: VIAN RAIES! The purpose of this lab exercise was to perform the bromination of (E)-1‚2-diphenylethene (trans-stilbene) by addition reaction in which bromine was added across the double bond to yield a vicinal dibromide. The next step was to perform a double elimination reaction by product gained to synthesize an alkyne‚ that is‚ 1‚2-diphenylacetylene. The two major techniques used in this lab were TLC analysis and UV-vis spectroscopy
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Hydrocinnamic acid underwent bromination using N-bromosuccinimide and AIBN. As one lab partner set up the reflux apparatus‚ the other measured the chemicals used in the lab experiment. 2.10 g of hydrocinnamic acid was used. It was observed as white and had a slight cinnamon smell. The amount of NBS was 2.49g and was measured in the fume hood. AIBN was measured at .030 g. 10 mL of acetic acid was also obtained. The reflux apparatus consisted of a 25 mL flask with a stir bar in a water bath. The chemicals
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6.1 ABSTRACT The densities (ρ) and viscosity (η) were reported for binary mixtures of N-methylformamide with O-substituted aniline (2-chloroaniline‚ 2-methylaniline and 2-methoxyaniline) over the entire composition range from 303.15 K to 318.15 K and at atmospheric pressure 0.1 MPa. These experimental data have been used to calculate excess volume (VE)‚ deviation in viscosity (∆η) and excess Gibbs energy of activation of viscous flow (G*E). The variations in these properties with composition for
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A Beautiful Mind with an Ugly Mental Disorder Submitted by: Nazila R. Salamkhail V-00410030 Psychology101-901 Instructor: Tim Donahue Virginia Commonwealth University 04/27/2011 The movie “A Beautiful Mind” is a fascinating movie. Although‚ I am not a movie watcher‚ it drew my full attention as soon as I started playing it. It displays the character of a great mathematician John Nash who is struggling with schizophrenia during his college period
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Organic Chemistry I LAB EXAM: FINAL BROMINATION OF BENZENE SYNTHESIS AND PURIFICATION OF BROMOBENZENE: PROCEDURE DATA TABLE Chemical Boiling point C Melting Point C Density g/mL Solubility Benzene 80.1 5.5 0.88 Slightly in H2O Toluene 110.6 -93 0.87 Slightly in H2O Bromobenzene 155-156 -30.8 1.50 Insoluble Dibromobenzene 220.40 87.31 0.96 Insoluble MATERIALS: Graduated cylinder Weight scale Buchner funnel Filter flask Rubber stopper Hot plate Thermometer Conical funnel Various
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LAB REPORT FOR EXPERIMENT #2: PURIFICATION OF ACETANILIDE BY RECRYSTALLIZATION Your name TA’s name Your Partner’s name Lab Section OBSERVATIONS: A. SELECTING A RECRYSTALLIZATION SOLVENT | |Solubility Test (cold) |Solubility Test (hot) | |Water |insoluble |soluble | |pet ether |insoluble
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group. The electrophilic aromatic substitution reaction nitration is used to nitrate methyl benzoate and acetanilide with a nitronium ion. Crystallization was used to purify the product. The melting point was used to determine its purity and the regiochemistry of the products. The methyl benzoate reaction product‚ methyl nitrobenzoate‚ was determined to be meta-substituted and the acetanilide reaction product‚ nitroacetanilide‚ was determined to be para-substituted. INTRODUCTION: An electrophilic
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