2.0 LITERATURE REVIEW
2.1 Polyurethanes
Polyurethane is an organic polymers, it was first discovered by Prof. Dr Otto Bayer in 1937. Polyurethanes are defined as polymers which contain urethane groups (-NH-CO-O-) in the main chain. However, as the versatility uses of this type of polymers, urethane group is not usually the principle group presents, other groups such as ester, ether, amine and urea groups are generally contained in the chain in reasonable number. Urethanes group present in the chain is the result from the reaction between molecules containing two or more hydroxyl (-OH) groups per molecules and isocyanates that have more than one reactive isocyanate group (-NCO) per molecule as for example reaction between diisocyanates with diol as shown in Figure 1. The reaction occurs in such a way hydrogen moves from diol to the nitrogen of diisocyanate while the oxygen of diol link with carbon on diisocyanate (Ophardt,
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Over the past decade, as the price of petroleum oil increased, the stability and the sustainability of the petroleum market have become serious concerns. Costs of polymeric raw materials have since risen due to increase in feedstock price (Zhang, Jeon, Malsam, Herrington, & Macosko, 2007). The conservation of environment from pollution is also taken into account in considering other alternative to petroleum based polyurthane as the number of wastes comes from polyurethane increase steadily as the production of it. The neutral-oil based polyurethane is known to be slightly or have potential to degrade compared to petroleum based polyurethane. In addition to the increasing waste cooking oil dumped illegally worldwide, studies had done on the potential of the waste cooking oil to be substituted as the raw material use in making
Abstract: In this experiment, triphenylmethanol was synthesized in two steps. First, the bromobenzene was reacted with dry magnesium turnings to produce Grignard reagent. Second, the Grignard reagent was reacted with methyl benzoate and concentrated sulfuric acid to produce an alcohol. The end result of the experiment was not very successful because only 17% yield of final product triphenylmethanol was recovered, and the final product was impure based on the melting point and the IR spectrum results.
The difference in this chemical and physical properties will aid in their separation. Processes like solubility, gravitational filtration and recrystallization will be used to separate the substances present in Panacetin. The melting and boiling point of the substances will help in concluding on which of these compounds will be presented at the end of experiment. Procedure and observation The Panacetin content was weighed approximately 3.0493g and transferred to the Erlenmeyer flask; 75ml of dichloromethane (CH¬2CL2) was added to the content. The dichloromethane (CH2Cl2) dissolved the sucrose, leaving the active unknown agent and aspirin behind.
The purpose of this lab is to determine the specific isomer of the bromovanillin produced. In this experiment, vanillin is brominated to produce a mixture of isomers or one single isomer of bromovanillin. The possible product(s) formed are 2-bromovanillin, 5-bromovanillin, and 6-bromovanillin, as seen in Figure 1.1 By utilizing the bromination process of vanillin, one bromovanillin isomer can be formed as a result. As the starting material, vanillin can work with various electrophilic aromatic substitution reactions, due to the presence of aromatic double bonds within the structure.
Their presence affects the reactivity and stability of dienes and dienophiles in the Diels-Alder reaction, making them more open. However, it allows the diene to reduce energy to produce a more stable cyclic product, but dienes with a low ring strain reduce reactivity in the reaction. Hexaphenylbenzene undergoes “ring closure” to form a new benzene ring. Ring closure is a reaction in which an open chain of atoms is closed to form a ring. The process includes breaking one of the carbon double bonds in the phenyl group and creating a new bond between the carbon atoms of the neighboring group, resulting in the hexaphenylbenzene creating a new ring.
These reactions could be distinguished from the others easily because the reaction would form gas bubbles and not solids. These reactions were also included in the
One of the reactions you observed resulted in this product: NaCl + H2O + CO2 (g)? What well did this reaction occur in? Describe how the observations for this reaction support your answer. B BoldI ItalicsU Underline Bulleted list Numbered list Superscript Subscript70 Words A reaction I observed in number 1.)
Lab Report 5: Acetylsalicylic Acid (Aspirin) Synthesis Name: Divya Mehta Student #: 139006548 Date Conducted: November 19th 2014 Date Submitted: November 26th 2014 Partner’s Name: Kirsten Matthews Lab Section: Wednesday 2:30 L9 IAs Name: Brittany Doerr Procedure: For the procedure, see lab manual (CH110 Lab Manual, Fall 2014) pages 96-98. Wilfrid Laurier University Chemistry Department. Fall 2014. Acetylsalicylic Acid (Aspirin) Synthesis.
The product obtained was (2S, 3R)-2, 3-dibromo-3-phenylpropanoic acid and (2R, 3S)-2, 3-dibromo-3-phenylpropanoic acid, which are enantiomers. This was determined through melting point analysis. The melting point range for the product was 198 to 202 degrees Celsius, which is a lot close to the given melting point of the anti-addition product, 202-204 degrees Celsius. The given melting point range was 93.5-95 degrees Celsius. Furthermore, the syn-addition product is unlikely and difficult to produce due to stereochemistry selectivity.
6.7, 6.8 Synthesis, Decomposition, and Displacement Reactions Kelly Mok SNC2DE-A Mr. Cox Partner: Nidhi S. Lab performed: September 18 & 19, 2014 Due: September 26, 2014 Purpose The purpose of this experiment is to observe and compare synthesis, decomposition, single displacement and double displacement reactions and the physical and chemical reactions that occur as a result. Hypothesis
Introduction: The purpose of this experiment is to demonstrate the different types of chemical reactions, those including Copper. There are different types of chemical reactions. A double displacement reaction is a chemical process involving the exchange of bonds between two reacting chemical species. A a decomposition reaction is the separation of a chemical compound into elements or simpler compounds and the single-displacement reaction is a type of
The objective of this experiment was to use an aldol condensation reaction to synthesize 3-nitrochalcone from 3- nitrobenzaldehyde. This was accomplished with a Diels-Alder reaction that utilized 3-nitrobenzaldehyde, acetophenone, ethanol, and sodium hydroxide. The mechanism for the synthesis of 3-nitrochalcone is presented in Figures 1 and 2. The alpha carbon on the acetophenone is deprotonated. This is followed by the attack of the alpha carbon anion on the carbonyl carbon on the 3-nitrobenzaldehyde.
The main objective of this experiment was the formation of phenacetin from the synthesis of acetaminophen. This was done through a chemical reaction known as the Williamson ether synthesis using techniques of refluxing, vacuum filtration and recrystallization incorporating a mixed solvent system. A further objective of this experiment was to study the formation of the product (phenacetin). Such validation was completed by using techniques for determining the melting point, calculating percent yield, and IR (infrared spectroscopy) of the resultant product.
C6H12 Possible side reactions: C6H6 + nH2 → cracking products C6H12 (benzene) ↔ C6H12 (methyl cyclo pentane) C6H6 + nH2 → C +
In this reaction Coenzyme A is needed. NADH is also created in this reaction. The NADH gives a hydride ion to the respiratory chain.
Major Facts Herman Miller is an internationally recognized furniture company founded in 1905. The company is deciding if they should continue to use polyvinyl chloride (PVC) in the manufacturing of the arm pads of their chairs. Arm pads are crucial in determining comfort for their customers and make up ten percent of the cost of the chair. Unfortunately, PVC goes against the company’s protocol because of the harmful chemicals it releases during production. Furthermore, Herman Miller international presence represents 15% of its sales and is predicted to be an important area for future growth.