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Bad White [126]
3 years ago
6

the increase of current when 15 V is applied to 10000ohm rheostat which is adjusted to 1000ohm value​

Engineering
1 answer:
Anastasy [175]3 years ago
4 0
Given data:
•) applied voltage = 15 V
•). Resistance = 1000 ohm

Required:
•). The magnitude of current= ?

•••••••••••••SOLUTION•••••••••••••

We can find the relation ship between current, voltage and resistance with the help of Ohms law.

According to ohms law;

V= IR.

Rearranging the above equation;

I= V/ R

Putt the values in the above equation; we get

I= 15V/ 1000ohm

I = 0.015 A( ampere)

••••••••••••••• CONCLUSION•••••••

The value of the current would be 0.15 ampere when Resistance is equal to 1000 and that of Voltage is equal to 15 V.
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From the following numbered list of characteristics, decide which pertain to (a) precipitation hardening, and which are displaye
Blababa [14]

Answer:

(a) Precipitation hardening

(1) The strengthening mechanism involves the hindering of dislocation motion by precipitates/particles.

(2) The hardening/strengthening effect is not retained at elevated temperatures for this process.

(4) The strength is developed by a heat treatment.  

(b) Dispersion strengthening

(1) The strengthening mechanism involves the hindering of dislocation motion by precipitates/particles.  

(3) The hardening/strengthening effect is retained at elevated temperatures for this process.

(5) The strength is developed without a heat treatment.  

7 0
3 years ago
If you stretch a rubber hose and pluck it, you can observe a pulse traveling up and down the hose. What happens to the speed of
stich3 [128]

Answer:

Explanation:if you stretch the hose more tightly the speed of the pulse will reduce..

5 0
3 years ago
A slender rod AB, of weight W, is attached to blocks A and B, which move freely in the guides shown. The blocks are connected by
gregori [183]

Answer:

(a) T = W/2(1-tanθ)  (b) 39.81°

Explanation:

(a) The equation for tension (T) can be derived by considering the summation of moment in the clockwise direction. Thus:

Summation of moment in clockwise direction is equivalent to zero. Therefore,

T*l*(sinθ) + W*(l/2)*cosθ - T*l*cosθ = 0

T*l*(cosθ - sinθ) = W*(l/2)*cosθ

T = W*cosθ/2(cosθ - sinθ)

Dividing both the numerator and denominator by cosθ, we have:

T = [W*cosθ/cosθ]/2[(cosθ - sinθ)/cosθ] = W/2(1-tanθ)

(b) If T = 3W, then:

3W = W/2(1-tanθ),

Further simplification and rearrangement lead to:

1 - tanθ = 1/6

tanθ = 1 - (1/6) = 5/6

θ = tan^(-1) 5/6 = 39.81°

8 0
3 years ago
The increasing interconnections of peoples and countries around the world is known as ________.
Irina18 [472]
I think it’s rationalization.
Hope this helps
4 0
3 years ago
Read 2 more answers
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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