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Compare And Contrast The Melting Point Of 4-Butoxyphenyl Acetamide

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The melting point that was observed for N-(4-butoxyphenyl)acetamide was 109.7˚C, and is lower than the literature value range of 131˚C. (Royal Society of Chemistry. 2018). This may be due to the presence of water and that impurities may be still present in the product that was formed. Solid substances that contain soluble impurities typically melts at a lower temperature than the pure compound (Kirsop. 2017). This is because the impurity disrupts the repeating pattern of forces that holds crystalline structure of the solid. A smaller amount of energy is required to melt the part of the solid surrounding the impurity, which supports that the compound that was produced was an impure compound.

To determine whether a reaction has been completed, …show more content…

SN1 reactions are dependent on the stability of the carbocations, where a tertiary carbocation is at its most stable form, causing a fast reaction rate (Hunt. 2009). The compound that had the highest rate of reaction of less than 1 min was 2-chloro-2-methyl propane, where benzene chloride followed (6 mins). The benzene chloride had a faster reaction than the other haloalkanes since the carbon that was attached to the chloride was connected to the benzene ring, in doing so quickens the reaction. Unlike the benzene chloride, chlorobenzene should have no reaction since the chlorine is directly attached to a carbon within the benzene ring. This unexpected result of having of having the solution turn cloudy may be due to a cross-contamination of the pipettes. The allyl chloride, had a slow reaction rate of 11 mins due to the carbocation being on a secondary carbon. The precipitate will eventually fully form, where this is the same case for the 2-chlorobutane and 1-chlorobutane as the carbocation is relatively unstable. Thus, causing the reaction to slowly occur and why no reaction was observed during the

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