Nitration of Acetanilide and Methyl Benzoate

Nitration of phenylacetamide and methyl radical BenzoateNitration of Acetanilide and Methyl Benzoate by Electrophilic Aromatic Substitution come upThe purpose of this experiment was to synthesize methyl radical nitro benzoate from methyl benzoate, as advantageously as nitro acetanilid from concentrated nitric venereal disease (HNO3), and concentrated sulfuric sulphurous (H2SO4) by utilise an electrophilic evocative substitution chemical response. The HNO3 and H2SO4 were combined to form a nitrating solution, which was added to a mixture of methyl benzoate and H2SO4, and the same was done with acetanilide. Fol mortifieding recrystallization, thawing head teacher was used to identify and characterize the ware of the reply. The thaw depute in time was dictated to be 74 C-80 C for methyl nitro benzoate and for nitroacetanilide it was 195 C-cc C, which indicates meta-regiochemistry for methyl benzoate and para-regiochemistry for nitroacetanilide. The portion flag of this reaction for the recrystallized product was 59.3% of methyl nitrobenzoate, period it was 6.75% for nitroacetanilide.Figure 1 The reaction for the nitration of acetanilide.Figure 2 The reaction for the nitration of methyl benzoate.Experimental tough sulfuric bliste make noise (0.6 mL) and concentrated nitric acid (0.5 mL) were added to a reaction flask and placed in an ice bath. Concentrated sulfuric acid (1 mL) was added to methyl benzoate (0.5 g) in a vial which was then packed in ice, and the same was done with acetanilide. While stirring, the cold H2SO4/HNO3 mixture was added drop-by-drop. After the acid mixture was added, the reaction mixture was removed from the ice to warm to get on temperature, with stirring. It was then transferred by Pasteur pipet into a beaker and stirred for five minutes. The methyl benzoate nitration organise clean solid, and the acetanilide nitration for a light yellow solid. The crystals were the inanity filtered with a Buchner funnel. The crude product was recrystallized by adding a distilled water and ethanol slowly while heating the product. While cooling, the solution produced large white crystals for methyl benzoate nitration and light yellow crystals for the acetanilide nitration. The mass, thawing point share yield were obtained.Results and DiscussionThrough the use of electrophilic aromatic substitution, acetanilide is nitrated to nitroacetanilide, while methyl benzoate was nitrated to methyl nitrobezonate. The first step of the reaction involved in the donation of an electron pair, which generates the nitronium ion from nitric acid by protonation and loss of water, using sulphuric acid as the dehydrating agent. The mechanics for methyl benzoate locoweed be seen below.Figure 3 The mechanism of the nitration of methyl benzoate to methyl nitrobenzoate.To prevent acetanilide from dinitrating, the nitrating solution of HNO3 and H2SO4 were added drop by drop to the acetanilide solution, so that the ingress of the ni trating agent is kept at minimum. The cooler temperatures were used to reduce the reaction rate and help to avoid over nitration.The electrophilic aromatic substitutions involved the successor of a proton on an aromatic ring with an electrophile that becomes substituent. The sulfuric acid protonates the methyl benzoate, which creates the resonance stabilized arenium ion intermediate.3 The electron deficient nitronium ion reacts with the protonated intermediate meta get. The ester congregation is the meta deactivator and the reaction takes place at the meta position because the ortho and para positions are destabilized by near validatings charges on the resonance structure.2 The major product of the methyl benzoate nitration is the meta product payable to carboxyl and nitro groups both being powerful electron withdrawing groups.Table 1 The weight, melting point, and percentage yield of both Nitroactenilide and Methyl Nitrobenzoate.Product call offCrude Weight (g)Product Weigh t (g)Percent Yield (%) dissolve Point (C)Literature Melting Point (C)Nitroactenilide0.5850.0456.75%195-200214-217Methyl Nitrobenzoate0.560.3259.3%74-8078-80The actual yield of methyl nitrobenzoate is 0.32 g while the theoretical yield is 0.54 g. The melting point is 74C 80C, and the esteem is closed to the literature value which is 78C 80 C. The percent yield for the methyl benzoate electrophilic aromatic substitution reaction was 59.3% with 0.32g of methyl nitrobenzoate formed. The percent yield for the reaction with acetanilide was 6.75% with 0.045g of nitroacetanilide formed, which can be seen in table 1. The melting point sight was 195-200 C, which can be accounted for impurities in the product, which can be seen below in table 1. Some impurities might be Ortho and Meta directing substances, as advantageously as there could contain been some experimental errors that occurred during the experiment such(prenominal) as not overheating solutions during the reactions. These low yields may have resulted from pitiful recrystallization, product lost during transfer from one apparatus to another, or forgiving error. The missing percent accounts for the impurities removed during recrystallization. However, some product must have been lost in the acetanilide reaction recrystallization because of such a low percent yield.The melting point of the final product was 74-80 C suggesting that it was formed by meta-substitution. The literature melting point for meta-methyl nitrobenzoate is 78-80 C. Therefore, the melting point is demean than it should be suggesting that an slag is in the product. This impurity may have occurred due(p) to poor recrystallization or it may have been picked up after recrystallization. The melting point of the nitroacetanilide product was 195-200 C suggesting the para-regiochemistry. The literature melting point for the p-nitroacetanilide is 214-217 C. Therefore, the melting point of the product is a little lower than the literature va lue, suggesting that an impurity exists in the product from poor recrystallization of contact with an impurity during recrystallization.The methyl nitrobenzoate product was determined to be meta-substituted based on its melting point range. This can also be proved by evaluating the attack of the benzol ring of methyl benzoate on the electrophililic species and nitric acid.4 The C-OCH3 substituent is a meta-deactivator. Therefore, when the benzene ring attacks the nitronium ion, the NO3+ group will add meta-positon. This creates a resonance stabilized arenium ion without a positive charge on the carbon with the C-OCH3 substituent. Then the proton is removed from the meta position by the weak base, the HSO4-, formed in the creation of the nitronium ion, which reforms the sulfuric acid catalyst.3 at once the proton is removed the substitution product, methyl nitrobenzoate remains.The nitroacetanilide product was formed by a para-substitution. This can be determined by examining the m elting point and study it to the literature values for each position.4 However, this can also be determined when examining the electrophilic aromatic substitution reaction of acetanilide on the electrophile, nitric acid. The NHCOCH3 substituent is an ortho-para-activator. Therefore, when the benzene ring of acetanilide attacks the nitronium ion, it can add ortho or para. The para substitution, if more(prenominal) stable than an ortho substitution, will be added because the para position is a save distance from the position of the NHCOCH3 substituent. Therefore, the benzene ring adds at the para position based on the melting point and resonance in the mechanism shown above.ConclusionThe methyl m-nitrobenzoate and p-nitroacetanilide were prepared. The percentage yield is 6.75% for nitroacetanilide and 59.3% for methyl nitrobenzoate. The melting point of the products are 74C 80C and 195C 200C. From the given physical constant, the literature melting point of methyl m-nitrobenzoate is 78 80C and 214C 217C for nitroacetailide, so it can be concluded that the products were methyl m-nitrobenzoate and p-nitroacetanilide.ReferencesWade, Jr., L.G. Organic Chemistry 2003, 722-741.Chemistry Laboratory manual of arms Susquehanna University 2014, 242-244 250ChemFinder.Com. Cambridge Soft Corporation. .Anerjee, Dhruv K. Ortho and Par % of Key Reaction. Utkarschemistry. 2013. cecal appendage A Finding the narrowing ReagentGrams X 1 bulwark / molecular weight = moles of reactantNitric acrimonious0.6 mL X ((1 g/1 mL) X 1 mol) / 98.08 g/mol = 0.0061 molNitric Acid0.5 mL X ((1 g/1 mL) X 1 mol) / 63.01 g/mol = 0.0079 molMethyl Benzoate(0.55 g X 1 mol) / 181.14 g/mol = 0.030 mol accessory B Calculating Theoretical Yield of Methyl NitrobenzoateMoles of limiting reagent X molar ratio X molecular weight of product) / 1 mol = theoretical yield(0.030 X 181.13) / 1 mol = 0.54 gAppendix C Calculating Percent Yield(Actual / theoretical) X 100% = percent yield(0.32 g/ 0.54 g) X 10 0% = 59.3%