1 Development of Poly-Cyclohexanone Resin Material for Coating Applications Appala Naidu Uttaravalli*, Srikanta Dinda Dept. of Chem. Engg., BITS?Pilani Hyderabad Campus, Hyderabad ? 500078, India *Corresponding author Email: uanaiduchemz@gmail.com Abstract: In the present work, polymerization reactions of cyclohexanone were carried out in a high pressure reactor. The effect of reaction parameters such as reaction time, temperature, and catalyst loading on hydroxyl value, iodine value, solubility, and average molecular weight of products was investigated. In the study, reaction time was varied from 10 17 hrs, reaction temperature was varied from 130 150 C, catalyst concentration was varied from 20 40%. The result shows …show more content…
Synthetic resin from cyclohexanone was first patented by BASF in 1930. Synthetic ketonic resins with different trade names like Laropal K80, MS2, AW2 and Ketone N are available for coating applications [1]. From the aforementioned literature survey, it has been observed that most of the studies were carried out on dimerization, trimerization and tetramerization reactions of cyclohexanone or alkyl cyclohexanone [2 5]. Very few studies are available in the literature on oligomerization or polymerization of cyclohexanone / alkyl cyclohexanone with aldehyde (mainly formaldehyde) to obtain a ketone aldehyde resin [6 9]. To the best of our knowledge, M/s. BASF Germany is the sole manufacturer of ketonic resins which are prepared from cyclohexanone and alkylated cyclohexanone [10 11]. Dinda et al. [12], have studied the self polymerization reaction of cyclohexanone using a high pressure reactor to prepare a solid resin. 2 Experimental Details 2.1 Materials In the present study, chemicals for synthesis such as cyclohexanone, methanol, and KOH were procured from S
The reaction was repeated 3 times and average rate noted. From these rates a graph was plotted which describes the relationship of the pressure produced and number of drops added. The reaction rates were measured by Kpa/min and were written to 4 figures for precise results. Time was measured by stop watch. Table 4 shows a summary of all the groups which participated in the lab session.
Act Two Scene V & Vl Major characters: Cyrano and Roxane Minor character(s): The Duenna Scene V Cyrano, Roxane, and the Duenna Cyrano: I’ll give her my letter with the slightest opportunity! (ROXANE, masked, appears behind the glass of the door, followed by the DUENNA. Cyrano goes to open the door.) Come in!
First, SUBOXONE is an prescription medicine, used as a treatment method for adults addicted to opioid drugs. Equally important, Suboxone is formulated as buprenorphine, which can be taken orally or sublingually in order to prevent pleasureable attempt of euphoria. By the same token, the medication SUBOXONE is an listed controlled substance containing buprenorphine, meant to target people abusing prescription medicines or street drugs. Another key point, Suboxone maintenance is an complete treatment program, which includes counseling and behavioral therapy.
Dalia El-Desoky Organic Chemistry II Lab 05 8 February 2017 Dehydration of 2-methylcyclohexanol Introduction: Dehydration is a common reaction in Organic Chemistry used to produce carbon-carbon double bonds. The dehydration mechanism involves the removal of water from an alcohol to form an alkene. In this experiment, 2-methylcyclohexanol will undergo acid catalyzed dehydration in heat to form three products: 1-methylcyclohexene, 3-methylcyclohexene, and methylenecyclohexane [1]. The reaction is carried out in a Hickman still filled with Drierite, a drying agent composed of CaSO4 which absorbs water.
The objective of this experiment was to perform a dehydration of 2-methylcyclohexanol. The result would be a mixture of 1-methylcyclohexene and 3-methylcyclohexene. There can also be a third product, methylenecyclohexane, though this would be identified using gas chromatography. An acid-catalyzed dehydration of 2-methylcyclohexanol occurs via an E1 mechanism; acids will react with 2-methylcyclohexanol to eliminate the alcohol (OH group). This causes the formation of a carbocation and an alkene will form near the charge.
There are several different reactions that can be used to synthesize an alkene product, however the main reaction being utilized for this experiment is the Wittig reaction and the Horner-Wadsworth-Emmons modification. The Wittig reaction involves a reaction between an aldehyde or ketone and ylid, which is also referred to as the Wittig reagent. The Wittig reagent is synthesized from a phosphonium salt and a strong base (Wittig Reaction, 2006). The reaction between the Wittig reagent and the ketone or aldehyde is a nucleophilic substitution; the carbon double bonded to the oxygen in the carbonyl is replaced with a carbon double bonded to another carbon (University of Liverpool, 2008).
Dehydration of 2-Methylcyclohexanol Sura Abedali Wednesday 2:00 PM January 31, 2018 Introduction: Dehydration reactions are important processes to convert alcohols into alkenes. It is a type of elimination reaction that removes an “-OH” group from one carbon molecule and a hydrogen from a neighboring carbon, thus releasing them as a water molecule (H2O) and forming a pi bond between the two carbons1. In this experiment, 2-methylcyclohexanol undergoes dehydration to form three possible products: methylenecylcohexane, 1-methylcyclohexene, and 3-methylcyclohexene in a Hickman still apparatus. Adding 85% Phosphoric Acid to protonates the “-OH” group, turning it into a better leaving group and initiating the dehydration reaction.
This summer, I was presented with the opportunity to read a classic book that goes by the name of Ethan Frome. At the beginning of the book, I was very lost and did not understand much of it because of the dialect that was being used in the book. As I kept reading it, I learned to accept it and I actually started to understand it a lot more. While reading this book, I had many thoughts about Ethan’s behavior, but my main thought was why would Ethan go and try to be with somebody else while he was already undoubtedly committed to a woman named Zeena?
After the assigned reaction was complete, samples of authentic cis-cyclohexene-1,2-diol, authentic trans-cyclohexene-1,2-diol, a 50:50 mix of the cis and trans cyclohexene-1,2-diols, and the product were each spotted on the Thin Layer Chromatography (TLC) plate. Then the TLC plate was placed inside a saturated beaker filled ethyl acetate in order to develop the plate. Once the solvent traveled up the solvent front, the plate was stained with anisaldehyde solution and then heated with a heat gun so the results could be visible. When looking at the results, the spot for the authentic cis-cyclohexene-1,2-diol turned a dark purple/light pink color, the spot for the authentic trans-cyclohexene-1,2-diol turned a light purple/blue color, the spot of the 50:50 mix of the cis and trans cyclohexene-1,2-diols turned a dark purple/light pink color, and the spot for the product turned a dark pink color. The color similarities between the product, the cis-cyclohexene-1,2-diol, and even the 50:50 mix of cis and trans diols indicated that the
The following lab period the solid was weighed (0.0483 g) and percent yield was calculated (65.5%) with the limiting reagent being tetraphenylcyclopentadienone. The melting point was determined. The first melting point was 204-204.9 °C and the second melting point was 215.6-215.9°C. Finally, an infrared spectroscopy was obtained for the
A white solid was formed as a product with 59.3% yield. In this reaction tetraphenylcyclopentadienone used as the diene, which was condensed with a highly reactive alkyne dienophile (diphenylacetylene). Heat was used to overcome the diene’s enhanced activation energy. The mixture turned dark brown indicated the loss of carbon monoxide, which made this reaction, overall, irreversible. The result was formation of a high yield hexaphenylbenzene which is more stable than the first product, The Reason is that the delocalized electrons in the rings give more stability to hexaphenylbenzene as compared to the dimethyl
The objective of this two-part experiment was to in Part I, create 4-tert-butylcyclohexanone via oxidation of 4-tert-butylcyclohexanol to provide a source of ketone for reduction procedures. Part II of the experiment was conducted preforming a series of reduction reactions in effort to asses the diastereoselectivity of aluminum isopropoxide (MPV reduction), sodium borohydride (NaBH4), and L-selectride when reacted with 4-tert-butylcyclohexanone. The methods used for analysis were TLC, IR, and 1HNMR spectroscopy. An oxidation of 4-tert-butylcyclohexanol was conducted to produce the ketone, 4-tert-butylcyclohexanone using oxidizing reagent, sodium hypochlorite in glacial acetic acid solvent.
Introduction Chevron Phillips Chemical Company is the major producer of Cyclohexane. This successful company hoses the three largest cyclohexane plants in the world. Many are puzzled by how the production of cyclohexane seems to have become stagnant. Perhaps this is due to the cost of benzene increasing or the demand increasing. Through thorough investigation, the answer to this question and many more can be answered.
Objective: The objective of the experiment is to synthesis cis-Norbornene-5,6-endo-Dicarboxylic anhydride in a Diels-alder reaction. The chemicals used are Maleic anhydride and Cyclopentadiene. In this experiment, the melting point and of cis-Norbornene-5,6-endo-Dicarboxylic anhydride is determine. Also, the percent yield.
The objective of this experiment was the synthesis of Isopentyl Acetate using an esterification reaction between acetic acid and Isopentyl Alcohol, using a strong acid as a catalyst. The product was washed, and distilled. This approach is called Fisher esterification, whereby esters are produced by refluxing a carboxylic acid and an alcohol in the presence of a concentrated acid catalyst. The ester produced had a banana smell odor. The extraction of the crude product was conducted using sodium bicarbonate followed by distillation.