All categories

3 years ago

Move the red warning icon to focus of the earthquake.

Chemistry

1 answer:

lina2011 [118]3 years ago

8 0

Answer:

Red goes in the spiky yellow box. Green goes where the red circles are. Blue goes in the small yellow box that is pointing to the line.

Explanation:

The focus of an earthquake is where it starts in the earth. The epicenter is the part directly above the focus on the surface. The fault is the part where the earth's crust splits.

You might be interested in

Help pleaseeeeeeeeeee

hichkok12 [17]

Answer:

D 1 and 3 only I am not sure

Explanation:

6 0

2 years ago

What is the viscosity and flammability of refinery gas?

Liono4ka [1.6K]

Hydrocarbons

Hope this helps :)

6 0

3 years ago

Assume a gasoline is isooctane, which has a density of 0.692 g/ml. What is the mass of 3.8 gal of the gasoline (1 gal = 3.78 l)?

sveticcg [70]

Density is the ratio of mass to the volume.

The mathematical expression is given as:

$density=\frac{mass}{volume}$

Now, density of isooctane = $0.692 g/mL$

Volume = $3.8 gal$

Since, 1 gallon = 3.78 L

So, 3.8 gal = $3.78 L\times 3.8$

= $14.364 L$

As, 1 L = 1000 mL

Therefore, $14.364 L$ = $14.364 L\times 1000 mL$

Volume in mL = $14364 mL$

Put the values,

$0.692 g/mL=\frac{mass}{14364 mL}$

$m = 0.692 g/mL\times 14364 mL$

= $9939.888 g$

Hence, mass of 3.8 gal of the gasoline is $9939.888 g$ .

6 0

3 years ago

What is the chemical name of the compound represented by the formula Ni2O3?

faust18 [17]

Answer:

Nickel(III) oxide is the chemical name of the compound represented by the formula Ni2O3?

3 0

3 years ago

According to markovnikov's rule of the electrophilic addition to an alkene, the electrophile, usually a proton, is more likely t

stealth61 [152]

According to markovnikov's rule of the electrophilic addition to an alkene, the electrophile, usually a proton, is more likely to add to the less-substituted carbon in a double bond.

With additional substituents present in this configuration, the intermediate carbocation is stabilised by being located on the more-substituted carbon.

The nucleophile will then end up in a double bond on the more-substituted carbon in a reaction that follows Markovnikov's rule.The outcome of some addition reactions is described by Markovnikov's rule or Markownikoff's rule in organic chemistry. Vladimir Markovnikov, a Russian scientist, created the rule in 1870.

To learn more about Markovnikov's rule

brainly.com/question/14529644

#SPJ4

8 0

2 years ago