Using Newman Projection, draw the eclipsed and gauche conformation of the following compounds. 1. propane (C1-C2)...

Using Newman Projection, draw the eclipsed and gauche conformation of the following compounds.

1. propane (C1-C2) CH₃CH₂CH₃

2. butane (C2-C3) CH₃CH₂CH₂CH₃

Why are both of the conformational isomers with a 0^o and 120^o dihedral angles considered to be in an eclipsed conformation?

Expert Solution

queen_honey_blossom answered 2 years ago

In Newman Projection, Draw the least stable conformation of propane. Then draw the most stable conformation...

In Newman Projection, Draw the least stable conformation of propane. Then draw the most stable conformation of propane

1. Draw the Newman projections for ethane and the C1-C2 bond of propane. 2. Which of...

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Draw the most stable conformer using a Newman projection for: Propane

-In a Newman projection formula of propane (staggered conformation), locate and describe any planes of symmetry...

-In a Newman projection formula of propane (staggered conformation), locate and describe any planes of symmetry and axes of symmetry. -In a Newman projection formula of propane (eclipsed conformation), locate and describe any planes of symmetry and axes of symmetry.

draw a Newman projection of the least stable eclipsed confirmer of 1 amino propane

Consider 2-methylpentane, (CH3)2CHCH2CH2CH3 (analyzing the C3-C4 bond): Draw a Newman projection for the Gauche conformation. Draw...

Consider 2-methylpentane, (CH3)2CHCH2CH2CH3 (analyzing the C3-C4 bond): Draw a Newman projection for the Gauche conformation. Draw a Newman projection for the Anti conformation. Draw the Newman projection for the highest energy conformation of the C3-C4 bond of 2-methylpentane.

For 1,4-dibromobutane(c2-c3) draw the newman projection for angle 0,60,120,180,240,300. Draw an energy graph. Why is one...

For 1,4-dibromobutane(c2-c3) draw the newman projection for angle 0,60,120,180,240,300. Draw an energy graph. Why is one staggered conformer more stable? Why is one staggered conformer least stable? Why is one of the eclipsed conformers more stable? Why is one of the eclipsed conformers least stable ?

Draw the Newman projection of the following compound, looking down the indicated bond. (2) Label this...

Draw the Newman projection of the following compound, looking down the indicated bond. (2) Label this Newman projections as a staggered or eclipsed conformation. (3) Rotate this Newman projection to draw the Newman projection of the most stable conformation of this compound. (3) Label this Newman projections as a staggered or eclipsed conformation. (4) Re-draw this most stable conformation in a wedge-dash form (as the original compound below is shown).

1. Solve for the optimal values of C1 and C2 in the following optimization problem: MaxC1,C2...

1. Solve for the optimal values of C1 and C2 in the following optimization problem: MaxC1,C2 C11/2 + βC21/2 s.t. C1 + C2 /1 + r = Y1 + Y2/1 + r Hint: ∂C1/2 /∂C = 1/2C−1/2 When r goes up, how does C1 change? Does it increase or decrease?

Consider the following 2-period model U(C1,C2) = min{3C1,4C2} C1 + S = Y1 – T1 C2...

Consider the following 2-period model U(C1,C2) = min{3C1,4C2} C1 + S = Y1 – T1 C2 = Y2 – T2 + (1+r)S Where C1 : first period consumption C2 : second period consumption S : first period saving Y1 = 20 : first period income T1 = 5 : first period lump-sum tax Y2 = 50 : second period income T2 = 10 : second period lump-sum tax r = 0.05 : real interest rate Find the optimal saving, S*

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