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vitfil [10]
2 years ago
13

11) If the evaporating pressure was 76 psig for r-22and the compressor inlet temperature was 65f, what would be the total superh

eat entering the compressor
Engineering
1 answer:
Karolina [17]2 years ago
7 0
Saturated Pressure Temperature chart for R-22 shows 45 degF at 76 psig
65-45= 20 degF superheat



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What are the benefits of using the engineering design process? combining scientific knowledge and creativity in a rigid and stru
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combining scientific knowledge, careful reasoning, and artistic invention in a flexible approach to problem-solving

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3 years ago
How would you describe what would happen to methane if the primary bonds were to break?
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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).

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When _____ ,the lithium ions are removed from the_____ and added into the _____
bezimeni [28]

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A 5-cm-diameter shaft rotates at 4500 rpm in a 15-cmlong, 8-cm-outer-diameter cast iron bearing (k = 70 W/m·K) with a uniform cl
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See explanation in the attached files

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