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Sav [38]
2 years ago
7

WHICH TASK BEST FITS THE ROLE OF A DESIGN ENGINEER ?

Engineering
1 answer:
pshichka [43]2 years ago
5 0

Answer: drafting blueprints

Explanation:

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1. A thin-walled cylindrical pressure vessel is capped at the end and is subjected to an internal pressure (p). The inside diame
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I DONT KNOW OKAY UGHHH
6 0
3 years ago
Engineers create a new metal that is stronger than steel but much lighter. This material is also significantly cheaper than what
zysi [14]

The best step for the engineers to make next is option D. Begin to design an airplane using this metal.

<h3>What is the metallic is plane parts?</h3>

Aluminum and its alloys are nevertheless very famous uncooked substances for the production of business planes, because of their excessive electricity at exceedingly low density. Currently, excessive-electricity alloy 7075, which includes copper, magnesium and zinc, is the only used predominantly withinside the plane industry.

The solution is D, due to the fact even as it's far crucial to marketplace the fabric and ensure humans are inquisitive about buying, they first want to attempt to layout aircraft the usage of this fabric. There isn't anyt any use promoting an aircraft constituted of this material_ if a aircraft can not be built.

Read more about the aircraft:

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7 0
2 years ago
A flat plate 1.5 m long and 1.0 m wide is towed in water at 20 o C in the direction of its length at a speed of 15 cm/s. Determi
beks73 [17]

Answer:

15.8

0.0944

Explanation:

L = 1.5

B = 1.0

Speed of water = 15cm

Temperature = 20⁰C

At 20⁰C

Specific weight = 9790

Kinematic viscosity v = 1.00x10^-4m²/s

Dynamic viscosity u = 1.00x10^-3

Density p = 998kg/m²

Reynolds number

= 0.15x1.5/1.00x10^-4

= 225000

S = 5

5x1.5/225000^1/2

= 0.0158

= 15.8mm

Resistance on one side of plate

F = 0.664x1x1.0x10^-3x0.15x225000^1/2

= 0.04724N

Total resistance

= 2N

= 2x0.04724

= 0.0944N

3 0
3 years ago
Engineering controls are the physical changes that employers make to the work environment or to equipment that make it safer to
____ [38]

Answer:

Engineering Controls. The best engineering controls to prevent heat-related illness is to make the work environment cooler and to reduce manual workload with mechanization. A variety of engineering controls can reduce workers' exposure to heat: Air conditioning, Increased general ventilation , Cooling fans , Local exhaust ventilation at points of high heat production or moisture, Reflective shields to redirect radiant heat , Insulation of hot surfaces Elimination of steam leaks , Cooled seats or benches for rest breaks , Use of mechanical equipment to reduce manual work, Misting fans that produce a spray of fine water droplets.

Hope this helped you!

Explanation:

5 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
3 years ago
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