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Alex777 [14]
3 years ago
5

g Using Newman projections, draw the most stable conformation for each of the following compounds. (a) 3-methyl pentane, viewed

along the C2-C3 bond (b) 3,3-dimethyl hexane, viewed along the C3-C4 bond
Chemistry
1 answer:
Marysya12 [62]3 years ago
3 0

Answer:

Using Newman projections, draw the most stable conformation for each of the following compounds.

(a) 3-methyl pentane, viewed along with the C2-C3 bond.

(b) 3,3-dimethyl hexane, viewed along with the C3-C4 bond.

Explanation:

(a) The structure of 3-methyl pentane is shown below:

In Newman projection, the most stable conformation is staggard conformation.

In staggard conformation, the torsional strain is very less compared to eclipsed conformation.

(b)3,3-dimethyl hexane, viewed along with the C3-C4 bond.

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As shown in table 15.2, kp for the equilibrium n21g2 + 3 h21g2 δ 2 nh31g2 is 4.51 * 10-5 at 450 °c. for each of the mixtures lis
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Our reaction balanced equation at equilibrium N2(g) + 3 H2(g) ↔ 2 NH3(g)
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when Kp = [P(NH3)]^2 / [P(N2)] * [P(H2)]^3
                = 98^2 / (45 * 55^3) = 1.28 x 10^-3
by comparing the Kp by the Kp at equilibrium(the given value) So,
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B) 57 atm NH3, 143 atm N2, no H2
∴ Kp = [P(NH3)]^2 / [P(N2)]
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c) 13 atm NH3, 27 atm N2, 82 atm H2
∴Kp = [P(NH3)]^2 / [P(N2)] * [P(H2)]^3
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∴ Kp< Kp equ (the given value)
∴it will shift rightward (to increase its value) towards porducts to achieve equilibrium.


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