Experiment Date: 3/12/2012 Photochemistry: Photoreduction of benzophenone and rearrangement to benzpinacolone Abstract: In this experiment Benzpinacolone was synthesized in a process that contained two steps. First the photoreduction of benzophenone in 2-propanol‚ which was done by placing the flask under sunlightfor the absorption of the UV rays to carry out the reaction. Then the second part was the dehydration of benzpinacol to benzpinacolone‚ where the benzpinacol product was converted
Premium
Lab Experiment 8: Oxidation Puzzle Post Lab Report for 2-ethyl-1‚3-hexandiol Calculations Theoretical yield: 1.857g Product Yield: 1.055g ----> Percent yield = (1.055g/1.87g) x 100% = 56.41% Starting amount of diol: 1.184g ----> Percent Yield = (1.184g/1.87g) x 100% = 63.32% Spectroscopy O-H (Stretch‚ H-bonded) C-H (Stretch) C-H (2720-2820 cm-1) Carbonyl C-O (Stretch) Product wavelength cm-1 3422 Strong‚ Broad 2877‚2936‚2964 Strong‚ Medium None Present 1705 Strong
Premium Alcohol Carboxylic acid Chlorine
wavelength Percentage concentration (methanol: water) Peak H value (height equivalent to a theoretical plate) (mm) 230nm 80:20 Phenol 0.0373 Benzophenone 0.0196 Naphthalene 0.0164 235nm 80:20 Phenol 0.0327 Benzophenone 0.0203 Naphthalene 0.0147 260nm 80:20 Phenol 0.0318 Benzophenone 0.0202 Naphthalene 0.0146 Figure 11: table for the height equivalent of the theoretical plates. It can be observed that the H values or height equivalent to a theoretical plate for phenol at the three wavelengths
Premium Chemistry Yield Stoichiometry
Research Article Vol: 2; Issue: 1 SYNTHESIS AND ANALYSIS OF BENZOPINACOL FROM BENZOPHENONE BY PHOTOREDUCTION IN GREEN CHEMISTRY. 1 Lata.C.Potey‚ 2* Dr. Satish B. Kosalge‚ 3 Rajeshwari S. Sarode 1 2 Assistant Professor‚ Hi-Tech College of Pharmacy‚ Chandrapur. Principal‚ Hi-Tech College of Pharmacy‚ Chandrapur 3 Assistant Professor‚ Hi-Tech College of Pharmacy‚ Chandrapur. Date Received: 11 TH Jan 2014 Date of Accepted: th 16 Jan 2014 Date Published: 18th
Premium Functional group Ethanol Chemical reaction
Review for exam II Exam for Wednesday (part A) General descriptions of organic molecules Saturated versus unsaturated molecules How to identify each and what properties each holds Given a molecular formula- draw all isomers possible Soluble or insoluble? Enantiomers‚ diastereomers‚ not isomers‚ cis/trans‚ etc Identify chiral centers Identify the compounds as being an acid‚ base or neither Hydrogen bonding‚ dipole-dipole interactions Rank several compounds by boiling point
Premium Oxygen Hydrogen Carbon
Distillation Objective: To illustrate the use of distillation for separating a mixture of two volatile liquids with different boiling points. Background: Distillation consists of heating a liquid until it vaporizes‚ and then condensing the vapor and collecting it in a separate container. Distillation is used to separate mixtures of liquids that either have different boiling points‚ or that have one component that does not distill. There are many types of distillation‚ each of which has a distinct
Premium Distillation
. Yes‚ comparably to TLC plate 2 and 3. The benzophenone is more neutral but as the same time its nonpolar‚ being that Silica gel in TLC 2 was polar and the solvent ethyl acetate-hexane is non-polar it moved relatively with the solvent. The stationary phase in TLC 3‚ alumina is non polar and the solvent ethyl acetate is polar so from the ideal that polar does not attract non-polar benzophenone stick stronger to alumina non-polar rather than moving up with polar solvent ethyl acetate as it did in
Premium Oxygen Solvent Acid
CHEM 2325 Organic Chemistry II Handout #1A – Alcohols 1) What type of orbital do the lone pair electrons on oxygen occupy in ethanol? A) σ B) π C) p D) sp E) sp3 2) Provide the structure of the major organic product in the reaction below. 3) Provide the structure of the major organic product in the reaction below. 4) Provide the structure of the major organic product in the reaction below. 5) Provide the structure of the major organic product in the reaction
Premium Alcohol Oxygen
Triphenylmethanol from Benzophenone Purpose: The purpose of this experiment was to synthesize the tertiary alcohol triphenylmethanol from a Grignard reagent‚ phenyl magnesium bromide. The Grignard reagent was synthesized from bromobenzene and magnesium and then reacted with benzophenone to produce triphenylmethanol. It was important that water be excluded from the reaction‚ in order to prevent the formation of benzene. The reaction of phenyl magnesium bromide and benzophenone was quenched with sulfuric
Premium Stoichiometry Magnesium
different melting point expected for the pure compound and a broadening of the melting point range. Such an observation would indicates that a compound is impure. In experiment 3.2‚ 0.120g sample of benzophenone was obtained from stock and crushed into a fine powder. Two samples of the benzophenone were loaded into a capillary tube. The capillary tubes were then individually placed in a Mel-Temp apparatus where they were gradually heated at a steady rate of 1º/minute. The melting rate was manually
Free Solid Liquid Temperature