The hydroxyl group (-OH) of NaOH attacks an electrophilic carbon of >N-C=O which as rearrangement gives carbonial . This carbonial abstract proton from water to give NAG. The established over degradation of NAG to 4-MBA was also obseved in alkali condition. Degradation pathway of AN is shown in Fig.3. The isolated degradation products are subjected to Mass studies to obtain their accurate mass fragment patterns.
1.2.2. Used as a solvent Butanol is an important solvent and can be used for the extraction of grease, pharmaceutical, and flavor. It has also been used as additives of alkyd resin and organic dyes, printing ink solvent, dew axing agent, coatings production, and pigment thinner. In addition, it has been used as flavoring spices of the
The goal of the experiment is to synthesize a bromohexane compound from 1-hexene and HBr(aq) under reflux conditions and use the silver nitrate and sodium iodide tests to determine if the product is a primary or secondary hydrocarbon. The heterogeneous reaction mixture contains 1-hexene, 48% HBr(aq), and tetrabutylammonium bromide and was heated to under reflux conditions. Heating under reflux means that the reaction mixture is heated at its boiling point so that the reaction can proceed at a faster rate. The attached reflux condenser allows volatile substances to return to the reaction flask so that no material is lost. Since alkenes are immiscible with concentrated HBr, tetrabutylammonium bromide is used as a phase-transfer catalyst.
SYSTEM SUITABILITY THEORETICAL PLATES: A standard solution of 25 µg mL-1of Amoxicillin trihydrate (in triplicate) was prepared and same was injected, then the system suitability parameters were calculated. Theoretical plates per meter Theoretical plates per meter were calculated from the data obtained from the peak using the following expression n = (5.54Vr2)/LWh2 Theoretical plates per column Theoretical plates column were calculated from the data obtained from the peak. n = (5.54Vr2)/Wh2 Where, ‘n’ is number of theoretical plates per meter, ‘Vr’ is the distance along the base line between the point of injection and a perpendicular dropped from the maximum of the peak of interest and ‘Wh’ is the width of the peak of interest at half peak
Polyester is synthetic fiber which mainly derive organic chemical compound from coal, air, water and petroleum and have the ester linkage. According to How (2015), the chemical reaction between an acid and alcohol formed polyester where a combination of two or more molecules form large molecule whose the structure repeats throughout its length. Researched by Smith (n.d) mentioned that production of polyester is by the chemical reaction of ethylene glycol with either terephthalic acid or its methyl ester in the presence of antimony catalyst to produce initially the monomer and low molecular mass oligomers. i. Starting from the acid: Direct esterification reaction.
1. For the demo experiment, the balanced chemical equation is as follows: (NH4)2Cr2O7(s)=Cr2O3(s)+N2(g)+4H2O(g). After the lightning of Ammonium dichromate, Chromium (III) oxide was formed while the Nitrogen and Water escaped into the atmosphere in a gaseous phase. Ammonium dichromate((NH4)2Cr2O7) gave rise to Chromium (III) oxide (Cr2O3), Nitrogen Gas(N2) and water (H2O) In terms of microscopic level, the ratio between reactants and products is as follows. One mole of Ammonium dichromate will give rise to one mole of 1 mole of Chromium (III) oxide and 1 mole of Nitrogen gas and 4 moles of Water is gaseous phase.
Lab Report 10: Nitration of Bromobenzene Raekwon Filmore CM 244 Section 40 March 27, 2018 Introduction: For this experiment, nitration of bromobenzene was the focus of the lab. The benzene is an aromatic compound and when it reacts with wither a mixture of sulfuric acid or nitric acid creates what is known as a nitro group. The formation of the nitro group is possible because it is an electrophilic aromatic substitution reaction. The creation of the nitronium ion is shown below: The reaction with the nitronium ion with bromobenzene creates three products instead of one. Depending on where the nitronium group or the alpha complexes of the reaction is on the ring, determines whether the product will be meta, para or ortho.
3.3. Synthetic methodologies for dihydropyrimidinones 3.3.1. Classical method Scheme-1: The conventional method for the synthesis of DHPMs is the one-pot three-component reaction of benzaldehyde, ethyl acetoacetate and urea in the presence of an acid catalyst. The product of this novel one-pot, three components synthesis that precipitated on cooling of the reaction mixture was identified as 3,4-dihydropyrimidin-2(1H)-one and this reaction came to be known as “Biginelli reaction”, or “Biginelli condensation”, or “Biginelli dihydropyrimidine synthesis” after the name of its inventor “Pietro Biginelli”.1 Mechanism Forty years after Biginelli’s initial report, the first mechanism for the synthesis of DHPMs was conducted by Folkers and Johnson
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. The dehydration of 2-methylcyclohexanol takes place at the bottom of the Hickman still.
Bromination is a type of electrophilic aromatic substitution reaction where one hydrogen atom of benzene or benzene derivative is replaced by bromine due to an electrophilic attack on the benzene ring. The purpose of this experiment is to undergo bromination reaction of acetanilide and aniline to form 4-bromoacetanilide and 2,4,6-tribromoaniline respectively. Since -NHCOCH3 of acetanilide and -NH2 of aniline are electron donating groups, they are ortho/para directors due to resonance stabilized structure. Even though the electron donating groups activate the benzene ring, their reactivities are different and result in the formation of different products during bromination. In acetanilide, the lone pair of the nitrogen is delocalized into the