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skelet666 [1.2K]
3 years ago
10

Phân tích phương pháp gia công plasma

Engineering
1 answer:
Irina-Kira [14]3 years ago
7 0

Answer:

can you plz write in English language so we can give you answer

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6-What is the difference between the critical point and the triple point?
hichkok12 [17]

Answer:

The triple point represents the combination of pressure and temperature that facilitates all phases of matter at equilibrium. The critical point terminates the liquid/gas phase line .

Explanation:

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Row choice the cost of roadway improvements to the developer and functional the amount of trafficBeing generated by the theater as well as the Ralph’s ladies
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3) Explain how dc machines Can work as motor and generator​
weeeeeb [17]

The working principle of a DC machine is when electric current flows through a coil within a magnetic field, and then the magnetic force generates a torque that rotates the dc motor. The DC machines are classified into two types such as DC generator as well as DC motor.

5 0
1 year ago
The annual inventory cost C for a manufacturer is given below, where Q is the order size when the inventory is replenished. Find
Nataly_w [17]

The change in annual cost when Q is increased from 340 to 341 is -1.23 and the instantaneous rate of change when Q = 340 is -1.25

<h3>How to find the Instantaneous rate of change?</h3>

The annual inventory cost C for a manufacturer is given as;

C = (1012000/Q) + 7.5Q

where Q is the order size when the inventory is replenished.

Now, the change in C can be calculated by evaluating the cost function at Q = 340 and Q = 341

Change in C = [1,012,000/341 + 7.5*341] - [1,012,000/340 + 7.5*340] ≈ -1.23

Instantaneous rate of change in C is first order derivative C':

C'(Q) = -1,012,000/(Q²) + 7.5

C'(340) = -1,012,000/(340²) + 7.5 ≈ -1.25

Read more about Instantaneous rate of change at; brainly.com/question/14666106

#SPJ1

8 0
1 year 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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