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Zigmanuir [339]
2 years ago
7

The product of the reaction between the following substances was treated with h2o. Draw the final product.

Chemistry
1 answer:
Viefleur [7K]2 years ago
5 0

Answer:

See explanation and picture

Explanation:

Question is incomplete, however, I found this question on several sites and most of them, have the same substances, so I'm gonna do it with that example to give you a hint of how to do it with yours, in case, it's a different substance.

First, we have a ketone and another substance, with MgCl. This is tipically the Grignard reagent, and this is often used to produce a tertiary alcohol.

The mechanism and final product is the following (See attached picture).

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It has been suggested that the surface melting of ice plays a role in enabling speed skaters to achieve peak performance. Carry
Fittoniya [83]

Answer:

a) Pf = 689.4 bar

b) P = 226.6 bar

c) T = 269.99 K

Explanation:

a)

The molar volume of ice is equal to:

Vi = m/p = (18.02x10^-3 kg H2O/1 mol H2O)*(1 m^3/920 kg) = 1.96x10^-5 m^3 mol^-1

The molar volume of liquid water is equal to:

Vl = (18.02x10^-3 kg/1 mol)*(1 m^3/997 kg) = 1.8x10^-5 m^3 mol^-1

The change in volume is equal to:

ΔVchange = Vi-Vl = 1.96x10^-5 - 1.8x10^-5 = 1.5x10^-6 m^3 mol^-1

using the Clapeyron equation:

Pf = Pi + ((ΔHf*ΔT)/(ΔVf*Ti)) = 1.013x10^5 Pa + ((6010 J mol^-1 * 4.7 K)/(1.5x10^-6 * 273.15 K)) = 6.89x10^7 Pa = 689.4 bar

b)

For the pressure we will use the equation:

P = (m*g)/A, where m is the mass, g is the acceleration of gravity and A is the area. Replacing values:

P = (79 kg * 9.81 m s^-2)/(1.9x10^-4 m * 0.18 m) = 2.26x10^7 Pa = 226.6 bar

c)

From Clapeyron´s expression we need to clear ΔT:

ΔT = ((Pf-Pi)*ΔV*Ti)/ΔHf = ((2.26x10^7 - 6.89x10^7)*1.5x10^-6*273.15)/6010 = -3.16 K

you can evaluate the new melting point of ice:

T = Ti + ΔT = 273.15 K - 3.16 K = 269.99 K

4 0
3 years ago
Why is it unnecessary to include an aluminum trihalide in electrophilic aromatic bromination reaction of acetanilide wih molecul
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Many electrophilic aromatic halogenations require the presence of an aluminum trihalide as a catalyst. We generally acetylated the amino group as protection. Now, this acetanilide can be brominated at Ortho or para position. An atom that is attached to an aromatic system usually hydrogen is replaced by an electrophile is an organic reaction which is called Electrophilic aromatic substitution. There are what you called important electrophilic aromatic substitutions they are aromatic nitration, aromatic sulfonation, aromatic halogenation and acylation and alkylating Friedel-Crafts reaction. Aromatic bromination is an electrophilic aromatic substitution (EAS) reaction, which will require benzene to act as a nucleophile to acquire an electrophile. Therefore, any directing groups that activate the ring will make it react more quickly with respect to aromatic bromination. Acetanilide is a moderately-activated ring <span>having a decent EWG.</span>
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