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Reika [66]
3 years ago
11

What combination of forces was the closest match? Why?

Chemistry
1 answer:
Virty [35]3 years ago
8 0

Answer: COMBINED FORCES

When forces act in the same direction, they combine to make a bigger force. When they act in opposite directions, they can cancel one another out. If the forces acting on an object balance, the object does not move, but may change shape.

Explanation:

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PLEASE HELP!
pogonyaev

Answer:

Q = 2.60 • 10^{3} J

Explanation:

Our specific heat capacity equation is:

Q = mC∆T

Q is the energy in joules.

m is the mass of the substance.

∆T is the temperature chance.

Let's plug in what we know.

  • We have 76.0 g of octane
  • The specific heat capacity of octane is 2.22 J/(g•K)
  • The temperature increases from 10.6º to 26.0º (a 15.4º increase)

Q = 76.0(2.22)(15.4)

Multiply.

Q = 2598.288

We want three significant figures.

Q = 2.60 • 10^{3}

or

Q = 2590 J

Hope this helps!

3 0
3 years ago
Read 2 more answers
1. Write formulas for the binary ionic compounds formed between
adell [148]

Answer:

a) KI

b) MgCl2

c) Na2S

d) Al2S3

e) AlN

Explanation:

8 0
3 years ago
Read 2 more answers
This is science help me pls
jek_recluse [69]
Remember velocity = distance/time so that mean you would do 60/3 which equals 20 so the speed(velocity) equals 20
6 0
2 years ago
Alkynes are reduced to trans alkenes by a process called dissolving metal reduction. The reaction uses sodium or lithium metal a
NISA [10]

Answer:

Explanation:

The movement of the electrons is illustrated in the picture attached to this answer. It is a four-step reaction mechanism.

First STEP: The first step involves the transfer of an electron from sodium to form a radical anion.

Second STEP: This radical anion then removes a proton/hydrogen from ammonia in a bid to neutralize itself (hence the hydrogen becomes bonded to the anion).

Third STEP: The sodium (from NaNH₂ formed) transfers an electron again to produce a vinyl carbanion.

Fourth STEP: The carbanion then removes a proton/hydrogen from ammonia (like in the second step) to form a neutral trans-alkene.

NOTE: The circled numbers denote each step while the mechanism on the left represents the use of any alkyl group (R and R') while the mechanism on the right assumes both alkyl groups are methyl. Hence, 2-butyne started the reaction and the final product was trans-2-butene.

6 0
3 years ago
Use the following graph of a car traveling on a straight northerly path to answer this question. At what time would the
BARSIC [14]

Answer:

B 144.0 s is the best answer of this question

6 0
4 years ago
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