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- 1. Which of the following compounds are constitutional isomers? 2. Which of the following is a wedge and dash structure for the following Newman projection?name and draw structural formulas for all cyclo-alkanes with the molecular formula C5H10. Be certain to include cis-trans isomers, as well as constitutional isomersThere are three cycloalkanes with no more than one substituent. Draw these three cycloalkanes in accordance with the ring size details provided below.Draw the structure of the cycloalkane with the largest ring below:
- Show the delocalization of charge in the following structure, draw the resonance forms and indicate the movement of electrons with a curved arrow CH2=CH-OThe reaction of chlorine with pentane gives a mixture of three chloroalkanes, each with the molecular formula C5HhC1. Write a line-angle formula and the 1UPAC name for each chloroalkane.Draw a potential-energy diagram for rotation about the C@2¬C@3 bond of pentane through 360°, starting with the least stable conformer.
- Draw Newman projections for the anti, eclipsed, gauche and fully eclipsed conformations of Butane. Indicate their relative stabilities and the reasons for your ranking-need to discuss the stresses involved in each case. Using suitable specific conformers of specific structures as examples, explain the difference between (a) angle strain (b) torsional strain and (c) steric strain. Need to draw the confomers and structures 4) Draw the most stable conformers using chair structures of the following: (c) cis-1,2-Dibromocyclohexane (d) trans-1,2-Dibromocyclohexane (e) cis-Decalin (f) trans-Decalin . Draw the most stable conformers of trans-1-Bromo-4-methylcyclohexane and cis-1-Bromo-4-methylcyclohexane. Which is more stable? Explain the reason for your answer. Need to include a discussion of 1,3-Diaxial interaction4. Draw the possible alkane compound with chemical formula C6H14 that contain:a) Primary and tertiary carbon only.Draw Newman projections for all staggered conformations formed by rotation from 0° to 360° about the carbon-carbon single bond.
- Complete the structual notations for alkanes shown below: (Lewis and Skeletal)C2H6CH3CH2CH3CH3CH2CH2CH3 CH3CH(CH3)CH3Citing down the C3-C4 bond, and using the drawings below, complete the Newman projections for all staggered and eclipsed conformations of hexane. Which staggered conformation has the lowest energy? Which eclipsed conformation has the highest energy?using newman projections draw the least and most stable conformations with respect to the bond indicated 1-hexyne (C3 is front carbon and C4 is back carbon)