The purpose of this particular experiment is to acquire the product 4-methylcyclohexene from the reactant 4-methylcyclohexanol by altering the equilibrium and using an elimination (E1) reaction involving dehydration with a strong acid acting as a catalyst. The following techniques and analyses were utilized in this experiment: simple distillation, “salting-out” the crude product, neutralization, unsaturation test, and infrared spectroscopy. Simple distillation is necessary for separating a liquid mixture and collecting the purified product or desired result. “Salting-out” the crude product was employed as a means of an extraction and purification process; that is, the salt would extract the water from the mixture, which leads to a reduction in solubility of the organic compound. …show more content…
The purpose of an unsaturation test (e.g. bromine test) is to identify compounds with carbon-carbon double bonds or triple bonds – since the desired product involves an alkene (by definition, has carbon-carbon double bonds), an unsaturation test would be a useful method for determining that structure. Infrared spectroscopy is a way to analysis the reactant and the product by creating plots of absorption bands and then using those bands of different variations (or locating discernible peaks) to identify the functional groups for that particular compound – this is a key way to make sure the correct product was obtained. The results of the unsaturation test and infrared spectroscopy would provide enough information to conclude whether this experiment was successful or not (i.e. if an alkene is present and the alcohol is
The goal of this two week lab was to examine the stereochemistry of the oxidation-reduction interconversion of 4-tert-butylcyclohexanol and 4-tert-butylcyclohexanone. The purpose of first week was to explore the oxidation of an alcohol to a ketone and see how the reduction of the ketone will affect the stereoselectivity. The purpose of first week is to oxidize the alcohol, 4-tert-butylcyclohexanol, to ketone just so that it can be reduced back into the alcohol to see how OH will react. The purpose of second week was to reduce 4-tert-butylcyclohexanol from first week and determine the effect of the product's diastereoselectivity by performing reduction procedures using sodium borohydride The chemicals for this lab are sodium hypochlorite, 4-tert-butylcyclohexanone
This week’s lab was the third and final step in a multi-step synthesis reaction. The starting material of this week was benzil and 1,3- diphenylacetone was added along with a strong base, KOH, to form the product tetraphenylcyclopentadienone. The product was confirmed to be tetraphenylcyclopentadienone based of the color of the product, the IR spectrum, and the mechanism of the reaction. The product of the reaction was a dark purple/black color, which corresponds to literature colors of tetraphenylcyclopentadienone. The tetraphenylcyclopentadienone product was a deep purple/black because of its absorption of all light wavelengths. The conjugated aromatic rings in the product create a delocalized pi electron system and the electrons are excited
The purpose of conducting experiment was to determine the identity of white compound. Based on the 5 gram of unknown white compound several experiment conducted including solubility test, pH test, flame test, and ion test. Several materials including chemicals used throughout experiment and will be described through paragraphs.
Hydration of alkenes is characterized by the addition of water and an acid-catalyst to a carbon-carbon bond leading to an alcohol. Dehydration is exactly the opposite in which dehydration of an alcohol requires water to be removed from the reactant. Equilibrium is established between the two processes when the rate of the forward reaction equals the rate of the reverse reaction. The alkene that is used in this experiment is norbornene. Through hydration of norbornene, an alcohol group should be present on the final product yielded what is known as exo-norborneol. Percent yield is a numerical indication of how much of the reactant was actually reacted to yield product. The equation for percent yield is shown below:
The sole purpose of performing the lab was to utilize aldol condensation reactions to synthesize a cyclopenta-dienone, while using UV spectrophotometry and computer visualization to further understand the dienone. In the beginning of the lab, the tetraphenylcyclopentadienone (TPCP) was synthesized using dibenzyl ketone and benzyl under extremely basic conditions. The synthesis process could be further understood by observing the mechanism portrayed in Figure 1. According to the figure, the dibenzyl ketone will first loose an alpha hydrogen to form the enolate intermediate.
Purpose/Introduction: In this experiment, four elimination reactions were compared and contrasted under acidic (H2SO4) and basic (KOC(CO3)3) conditions. Acid-catalyzed dehydration was done on 2-butanol and 1-butanol; a 2o and 1o alcohol, respectively. The base-induced dehydrobromination was performed on 2-bromobutane and 1-bromobutane isomeric halides. The stereochemistry and regiochemistry of the four reactions were analyzed by gas chromatography (GC) to determine product distribution (assuming that the amount of each product in the gas mixture is proportional to the area under its complementary GC peak).
Perchloroethylene (PCE), along with Trichloroethylene (TCE), are the products of the chlorination of Ethylene Dichloride (EDC). This process involves the reaction of EDC with chlorine, where its products undergo further distillation and purification to produce TCE and PCE fit for consumerism trade. The stoichiometry of the given process reaction indicates which is the greater desired product, i.e. either PCE or TCE. The reaction takes place at a temperature of 400 – 450 degrees Celsius and a pressure of 1 atmosphere.
Chlorinated hydrocarbon - name it, describe its route of entry, and 1 or 2 health effects
The goal of this experiment is to determine which products are formed from elimination reactions that occur in the dehydration of an alcohol under acidic and basic conditions. The process utilized is the acid-catalyzed dehydration of a secondary and primary alcohol, 1-butanol and 2-butanol, and the base-induced dehydrobromination of a secondary and primary bromide, 1-bromobutane and 2-bromobutane. The different products formed form each of these reactions will be analyzed using gas chromatography, which helps understand stereochemistry and regioselectivity of each product formed.
In a small reaction tube, the tetraphenylcyclopentadienone (0.110 g, 0.28 mmol) was added into the dimethyl acetylene dicarboxylate (0.1 mL) and nitrobenzene (1 mL) along with a boiling stick. The color of the mixed solution was purple. The solution was then heated to reflux until it turned into a tan color. After the color change has occurred, ethanol (3 mL) was stirred into the small reaction tube. After that, the small reaction tube was placed in an ice bath until the solid was formed at the bottom of the tube. Then, the solution with the precipitate was filtered through vacuum filtration and washed with ethanol. The precipitate then was dried and weighed. The final product was dimethyl tertraphenylpthalate (0.086 g, 0.172mmol, 61.42%).
The purpose of this experiment was to learn and preform an acid-base extraction technique to separate organic compounds successfully and obtaining amounts of each component in the mixture. In this experiment, the separation will be done by separatory funnel preforming on two liquids that are immiscible from two layers when added together. The individual components of Phensuprin (Acetylsalicylic acid, Acetanilide, and Sucrose as a filler) was separated based upon their solubility and reactivity, and the amount of each component in the mixture was obtained. Also, the purity of each component will be determined by the melting point of the component.
Saturated sodium chloride solution, also known as brine solution, is used to wash the distillate mixture. The distillate mixture is the phosphoric acid the co-distilled with the product. The brine solution also removes most of the water from the 4-methylcyclohexane layer. When six drops of 4-methylcyclohexene were added with two
Chloromethane, more commonly referred to as methyl chloride, is an organic compound categorized as a haloalkane functional group. Functional groups are atoms that control how the molecule will react with other molecues. Haloalkane functional groups consist of a carbon atom with four single bonds and one of the bonds in occupied by an element in the Halogen family; in this case chlorine. The structural formula is CH3Cl. This formula effects some of the physical properties which include the boiling point to be -22.22°C and the melting point to be -97.7°C. Other physical properties consist of a faint sweet smell, colorless gas, and it is soluble in water.
- The amount of times the mixture was stirred. We stirred the mixture until the Ammonium Nitrate was dissolved, so the amount of times we stirred after each teaspoon was different.
The chloroform and methanol for sample preparation and the acetic acid (CH3COOH) used in the mobile phase were of A standard of analytical reagent (AR