Question 3 (a) Build and draw by hand (on a paper and take photo of your drawing and paste it on the MS Word document with all other answers) the two different chair forms of methylcyclohexane (equatorial and axial). (b) How would you describe the relationship between these two molecules? (c) Which chair form of the methylcyclohexane is more stable? Why? (d) Can you interconvert these two different forms of methylcyclohexane without breaking a bond? How? (e) Using the chair equatorial methylcyclohexane model, convert this chair form to a boat form (without breaking a bond) by moving only C-4 up or down (C-1 is the carbon bearing the methyl group). Draw by hand (on a paper and take photo of your drawing and paste it on the MS Word document with all other answers) this boat form and call it as molecule (E). Explain why this is less stable than the chair equatorial methylcyclohexane. (f) Using the chair axial methylcyclohexane model convert this chair form to a boat form (without breaking a bond) by moving only C-4 up or down (C-1 is the carbon bearing the methyl group). Draw by hand (on a paper and take photo of your drawing and paste it on the MS Word document with all other answers) this boat form and call it as molecule (F). Explain why this is less stable than the chair equatorial methylcyclohexane. Which boat form (E or F) is less stable? Explain briefly