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 ?

Expert Solution

Why is one staggered conformer more stable?

In the above figure one of the staggered conformer is more stable because the more bulky groups (CH₂Br) are arranged far away from each other.

Why is one staggered conformer least stable?

In one staggered conformer is less stable because the more bulky groups are arranged close to each other.

Why is one of the eclipsed conformers more stable?

One of the eclipsed structure is more stable because the bulkier group (CH₂Br) is elipsed with H

Why is one of the eclipsed conformers least stable ?

One of the eclipsed structure is least stable because the two bulkier group (CH₂Br) is elipsed..

queen_honey_blossom answered 2 years ago

Please do the Projetion of Newman (C2 – C3) and the Projetion of Newman (C2 –...

Please do the Projetion of Newman (C2 – C3) and the Projetion of Newman (C2 – C3) of Butane and the 2-metilpropane Projection of Newman (C2 –C3) Projection of Newman (C2 –C3)

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.

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 0o and 120o dihedral angles considered to be in an eclipsed conformation?

An energy-dihedral angle diagram is provided for molecule Butane C4H10. Choose the right corresponding newman projection...

An energy-dihedral angle diagram is provided for molecule Butane C4H10. Choose the right corresponding newman projection for the circled energy state. What is the newman projection for 1? 2 What is the newman projection for 2? What is the newman projection for 3? What is the newman projection for 4?

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

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

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

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).

Using the newman projection of n-butane. construct an energy diagram to show the varation in free...

Using the newman projection of n-butane. construct an energy diagram to show the varation in free energy of n-butane as the dihedral angle made by C1-C2-C3-C4 is changed from 0 degrees to 360 degrees in 60 degree increment.begin with a staggered conformation and to acquire the eclipse . Rotating in 60 degree increment draw the energy change. draw the newman projection for each conformation. what is the energy difference between the two most stable conformations.

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

1. Draw the Newman projections for ethane and the C1-C2 bond of propane. 2. Which of the projection in #1 would have the highest energy? Why? 3. A chiral molecule requires a stereogenic center. What must be true about a carbon atom in a molecule for it to be a stereogenic center? 4. Based on the answer to #3, Draw the smallest acyclic chiral alkane and using wedges, show it in the S configuration.

Question