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Alecsey [184]
2 years ago
10

Is the COP of a heat pump always larger than 1?

Engineering
1 answer:
Liono4ka [1.6K]2 years ago
3 0

Answer:

Yes

Explanation:

Yes it is true that COP of heat pump always greater than 1.But the COP of refrigeration can be greater or less than 1.

We know that

COP of heat pump=  1 + COP of refrigeration

It is clear that COP can not be negative .So from the above expression we can say that COP of heat pump is always greater than one.  

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An amplifier with 40 dB of small-signal, open-circuit voltage gain, an input resistance of 1 MO, and an output resistance of 100
Vanyuwa [196]

convert 40db to standard gain

AL=10^40/20=100

calculate total voltage gain

=AL×RL/RL+Ri

=83.33

38.41 DB

calculate power

Pi=Vi^2/Ri Po=Vo^2/RL

power gain= Po/Pi

=13.90×10^6

3 0
3 years ago
Airbags will deploy in a head on collision but not in a collision that occurs from angle
Aneli [31]

Answer:  

Airbags will deploy in almost any angle.

Explanation:

Cars have sensors around them, so when the car gets hit, the sensors detect a crash and deploy the airbags to keep you safe.

8 0
3 years ago
A 60-cm-high, 40-cm-diameter cylindrical water tank is being transported on a level road. The highest acceleration anticipated i
dlinn [17]

Answer:

h_{max} = 51.8 cm

Explanation:

given data:

height of tank = 60cm

diameter of tank =40cm

accelration = 4 m/s2

suppose x- axis - direction of motion

z -axis - vertical direction

\theta = water surface angle with horizontal surface

a_x =accelration in x direction

a_z =accelration in z direction

slope in xz plane is

tan\theta = \frac{a_x}{g +a_z}

tan\theta = \frac{4}{9.81+0}

tan\theta =0.4077

the maximum height of water surface at mid of inclination is

\Delta h = \frac{d}{2} tan\theta

            =\frac{0.4}{2}0.4077

\Delta h  0.082 cm

the maximu height of wwater to avoid spilling is

h_{max} = h_{tank} -\Delta h

            = 60 - 8.2

h_{max} = 51.8 cm

the height requird if no spill water is h_{max} = 51.8 cm

3 0
3 years ago
What is (10 to the power of three) times (3 to the power of 10)? will give brainliest
VLD [36.1K]

59,049,000 is the answer.

7 0
3 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
2 years ago
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