1answer.
Ask question
Login Signup
Ask question
All categories
  • English
  • Mathematics
  • Social Studies
  • Business
  • History
  • Health
  • Geography
  • Biology
  • Physics
  • Chemistry
  • Computers and Technology
  • Arts
  • World Languages
  • Spanish
  • French
  • German
  • Advanced Placement (AP)
  • SAT
  • Medicine
  • Law
  • Engineering
kvasek [131]
3 years ago
8

You have 255 mL of a 1.5 M solution, how much liquid do you need to BOIL AWAY to increase the molarity to 2.5 M?

Chemistry
1 answer:
Lera25 [3.4K]3 years ago
6 0

Answer:

102ml

Explanation:

  1. by using the dilution formulae and then you slove for the second volume by making it subject of the fomular
  2. when you get it you then subtract the final volume that you got from the initial volume because they asked from the question what liquid do u need to boil away
You might be interested in
The magnitude of an earthquake is its:
Umnica [9.8K]

Answer:

25 size or length.

<h2>26 P wave (primary wave)</h2><h2>27 P wave</h2><h2>28 Surface waves</h2><h2>29 Body waves</h2><h2>30 Epicentre </h2><h2>31 Epicentre </h2><h2>32 Oxidation</h2><h2>33 Mineral Fragments </h2><h2>34 C.</h2><h2>35 C.</h2><h2>36 Transpiration.</h2><h2>37 . infiltration </h2><h2>38. 0.3</h2><h2>39.C</h2><h2>40.D.</h2><h2>41.D.</h2><h2>42.B.</h2><h2>4 3 . weathering </h2>

7 0
3 years ago
10. the answer is not D , I know for a fact
Cerrena [4.2K]
A I have a periodic table with me I checked
8 0
3 years ago
Can someone plz help me?
hichkok12 [17]
C would be the answer
8 0
4 years ago
Which statement is incorrect regarding the reaction of benzene with an electrophile? View Available Hint(s) A) The carbocation i
Leno4ka [110]

Answer:

The carbocation intermediate reacts with a nucleophile to form the addition product.

Explanation:

The reaction of benzene with an electrophile is an electrophillic substitution reaction. Here the electrophile replaces hydrogen. There is no formation of carbocation as intermediate in the reaction. Infact there is transition state where the electorphile attacks on benzene ring and at the same time the hydrogen gets removed from the benzene. So a transition carbocation is formed.

The general mechanism is shown in the figure.

i) Attack of the electrophile on the benzene (which is the nucleophile)

ii) The carbocation intermediate loses a proton from the carbon bonded to the electrophile.

iii) the carbocation formation is the rate determining step.

iv) There is no formation of addition product.

Thus the wrong statement is

The carbocation intermediate reacts with a nucleophile to form the addition product.

3 0
4 years ago
How is energy from grass passed on between animals
TEA [102]

Answer:

An animal will eat the grass and the energy then gets passed through the food chain

Explanation:

6 0
3 years ago
Read 2 more answers
Other questions:
  • How are cells similar to a factory or a business? List five similarities
    5·2 answers
  • What is the melting point of gallium?
    12·2 answers
  • A sample compound contains 5.723g Ag, 0.852g S and 1.695g O. Determine its empirical formula.
    11·2 answers
  • Identify the state of matter for A, B, and C.
    7·1 answer
  • According to the image, identify the number of neutrons in the most common isotope of aluminum. A) 13 B) 14 C) 26 D) 27
    5·2 answers
  • In a typical fireworks device, the heat of the reaction between a strong oxidizing agent, such as KClO₄, and an organic compound
    5·1 answer
  • Which law relates to the ideal gas law?
    12·1 answer
  • Can someone plz help me with this..
    12·1 answer
  • Is vineasel edible??????????????????????/
    5·2 answers
  • What is the molarity of a solution when 2.75 g of NaCl is dissolved in 1100 mL of solution?
    11·1 answer
Add answer
Login
Not registered? Fast signup
Signup
Login Signup
Ask question!