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strojnjashka [21]
2 years ago
13

How can you drop two eggs the feweHow can you drop two eggs the fewest amount of times, without them breaking? ...st amount of t

imes, without them breaking? ...
Engineering
2 answers:
Lesechka [4]2 years ago
8 0

Answer:

How can you drop two eggs the fewest amount of times, without them breaking it

Explanation:

This is done on any floor, the highest or the lowest. Simply drop the egg from one inch above your foot and it will not break.

AveGali [126]2 years ago
3 0

Answer:

answer

Explanation:

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The intake and exhaust processes are not considered in the p-V diagram of Otto cycle. a) true b) false
vovangra [49]

Answer:

b) false

Explanation:

We know that Otto cycle is the ideal cycle for all petrol working engine.In Otto cycle all process are consider is ideal ,means there is no any ir-reversibility in the processes.

It consist four processes

1-2:Reversible adiabatic compression

2-3:Constant volume heat addition

3-4:Reversible adiabatic expansion

3-4:Constant volume heat rejection

Along with above 4 processes intake and exhaust processes are parallel to each other.From the P-v diagram we can see that all processes.

But actually in general we are not showing intake and exhaust line then it did not mean that in Otto cycle did not have intake and exhaust processes.

6 0
3 years ago
Refrigerant-134a enters a 28-cm-diameter pipe steadily at 200 kPa and 20°C with a velocity of 5 m/s. The refrigerant gains heat
Alexandra [31]

Answer:

V = 0.30787 m³/s

m = 2.6963 kg/s

v2 =  0.3705 m³/s

v2 = 6.017 m/s

Explanation:

given data

diameter = 28 cm

steadily =200 kPa

temperature = 20°C

velocity = 5 m/s

solution

we know mass flow rate is

m = ρ A v

floe rate V = Av

m = ρ V

flow rate = V = \frac{m}{\rho}

V = Av = \frac{\pi}{4} * d^2 * v1

V = \frac{\pi}{4} * 0.28^2 * 5

V = 0.30787 m³/s

and

mass flow rate of the refrigerant is

m = ρ A v

m = ρ V

m = \frac{V}{v} = \frac{0.30787}{0.11418}

m = 2.6963 kg/s

and

velocity and volume flow rate at exit

velocity = mass × v

v2 = 2.6963 × 0.13741 = 0.3705 m³/s

and

v2 = A2×v2

v2 = \frac{v2}{A2}

v2 = \frac{0.3705}{\frac{\pi}{4} * 0.28^2}

v2 = 6.017 m/s

7 0
3 years ago
To solve the problem, make assumptions for missing data and justify. Given:
finlep [7]

Answer:

5,4,1, this is a explication

6 0
2 years ago
Car B is traveling a distance dd ahead of car A. Both cars are traveling at 60 ft/s when the driver of B suddenly applies the br
vagabundo [1.1K]

Answer:

Explanation:

Using the kinematics equation v = v_o + a_ct to determine the velocity of car B.

where;

v_o = initial velocity

a_c = constant deceleration

Assuming the constant deceleration is = -12 ft/s^2

Also, the kinematic equation that relates to the distance with the time is:

S = d + v_ot + \dfrac{1}{2}at^2

Then:

v_B = 60-12t

The distance traveled by car B in the given time (t) is expressed as:

S_B = d + 60 t - \dfrac{1}{2}(12t^2)

For car A, the needed time (t) to come to rest is:

v_A = 60 - 18(t-0.75)

Also, the distance traveled by car A in the given time (t) is expressed as:

S_A = 60  * 0.75 +60(t-0.75) -\dfrac{1}{2}*18*(t-0.750)^2

Relating both velocities:

v_B = v_A

60-12t = 60 - 18(t-0.75)

60-12t =73.5 - 18t

60- 73.5 = - 18t+ 12t

-13.5 =-6t

t = 2.25 s

At t = 2.25s, the required minimum distance can be estimated by equating both distances traveled by both cars

i.e.

S_B = S_A

d + 60 t - \dfrac{1}{2}(12t^2) = 60  * 0.75 +60(t-0.75) -\dfrac{1}{2}*18*(t-0.750)^2

d + 60 (2.25) - \dfrac{1}{2}(12*(2.25)^2) = 60  * 0.75 +60((2.25)-0.75) -\dfrac{1}{2}*18*((2.25)-0.750)^2

d + 104.625 = 114.75

d = 114.75 - 104.625

d = 10.125 ft

3 0
2 years ago
How would you describe what would happen to methane if the primary bonds were to break?
erastova [34]

Answer:

All the bonds in methane (CH4CH4) are equivalent, and all have the same dissociation energy.

The product of the dissociation is methyl radical (CH3CH3). All the bonds in methyl radical are equivalent, and all have the same dissociation energy.

The product of that dissociation is methylene (CH2CH2). All the bonds in methylene are equivalent, and all have the same dissociation energy.

The product of that dissociation is methyne (CHCH) .

The C-H bonds in methane do not have the same dissociation energy as C-H bonds in methyl radical, which in turn do not have the same dissociation energy as the C-H bonds in methylene, which are again different from the C-H bond in methyne.

If (by some miracle) you were able to get all four bonds in methane to dissociate absolutely simultaneously, they would all show the same dissociation energy… but that energy, per bond broken, would be different than the energy required to break just one C-H bond in methane, because the products are different.

(In this case, it’s CH4→C+4HCH4→C+4H versus CH4→CH3+HCH4→CH3+H.)

To alter hydrocarbons you add enough energy to break a C-H bond. Why does only one bond break? What concentrates the energy on one C-H bond?

the weakest CH bond is the one that breaks. in plain alkanes it has to do with the molecular orbital interactions between neighboring carbon atoms. look at propane for example. the middle carbon has two C-C bonds, and each of those C-C bonds is strengthened by slight electron delocalization from the C-H bonds overlapping with the antibonding orbitals of the adjacent carbons.

since the C-H bonds on the middle carbon donate electron density to both of its neighbors, those two are weakest.

one of them will break preferentially.

which one actually breaks depends on the reaction conditions (kinetics). frankly it's whichever one ramdomly approaches a nucleophile first. when the nucleophile pulls of one of the H's, the other C-H bonds start to share (delocalize) the negative charge across the whole molecule. so while the middle C feels the majority of the negative charge character, the other two C's take on a fair amount as well...

by the way, alkanes don't really like to break and form anions like that.

a better example would be something like isopropyl iodide, where the C-I bond breaks and the I carries away the electron pair, forming a carbocation (also not particularly stable, but more so than the carbanion).

7 0
3 years ago
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