Question 1 a) Benzenecarboxylic acid, commonly known as benzoic acid, has a pK₁ of 4.20. Find the pH of a 0.20 M solution of benzoic acid. b) Elemental analysis showed that a compound X had the empirical formula C6H7N. A simplified mass spectrum of X is shown below, together with an IR spectrum. Relative Intensity 120 100 80 20 1.0 0.8 0.2 0.0 10 16 3500 20 3000 2500 50 m/2 60 Infrared Spectrum 2000 70 1500 77 80 1000 90 93 92 M iv) A chemist reacted X with benzoyl chloride to produce a new organic compound, Y. Outline the mechanism of this reaction and clearly label compound Y. Wavenumbers (cm-1) i) Suggest chemical fragment identities for the mass spectrum peaks at m/z = 16 and m/z = 77 ii) Suggest chemical bond identities for the peaks at approx. (3400 and 3500) cm-¹ and (1500 and 1600) cm-¹. iii) Use your answers to i) and ii) to identify compound X and draw its structure. Include its IUPAC name. 10 500
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A,b and i please

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