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hjlf
3 years ago
6

HELP ME ILL MARK BRAINLIESTTTT PLSS ASAP

Chemistry
2 answers:
krok68 [10]3 years ago
8 0

Answer:

I think w but I don't know

Alenkasestr [34]3 years ago
7 0

Answer:

y

Explanation:

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Rank the solutions below in order of increasing acidity. (Drag and drop into the appropriate area)
Vladimir79 [104]

Answer:

0.1 M NaOH, 3 M NH3, 0.01 M CH3COOH, 0.01 M H2SO4, 0.1 M HCl

Explanation:

Strong acids are more acids than weak acids. In the same way, strong bases are more basic than weak bases that are in the same concentration.

Then, the more concentrated acid or base will be more acidic or basic.

CH3COOH. Weak acid

NaOH. Strong base

H2SO4. Strong acid

NH3. Weak base.

HCl. Strong acid

The less acid (More basic):

<h3>0.1 M NaOH, 3 M NH3, 0.01 M CH3COOH, 0.01 M H2SO4, 0.1 M HCl</h3>

Strong base, weak base, weak acid, diluted strong acid, undiluted strong acid

7 0
3 years ago
All isotopes of a particular element have the same atomic number. how then do the isotopes of a particular element differ?
White raven [17]
They have less or more neutrons. Isotopes have same number of protons but different number of neutrons.
4 0
3 years ago
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What's the purpose of mitosis and meiosis?
krok68 [10]
The purport of mitosis is cell regeneration, magnification, and asexual reproduction,while the purport of meiosis is the engenderment of gametes for sexual reproduction. Mitosis is a single nuclear division that results in two nuclei that are conventionally partitioned into two incipient daughter cells.
4 0
3 years ago
Which of the following is an essential condition for a combustion reaction ?
Ugo [173]
B is the answer to your question
8 0
3 years ago
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Which of the following is a likely mechanism for the reaction CH3Cl + OH- ----&gt; CH3OH + Cl-, which is first order with respec
abruzzese [7]

Answer:

A one-step mechanism involving a transition state that has a carbon partially bonded to both chlorine and oxygen

Explanation:

The compound CH3Cl is methyl chloride. This is a nucleophilic substitution reaction that proceeds by an SN2 mechanism. The SN2 mechanism is a concerted reaction mechanism. This means that the departure of the leaving group is assisted by the incoming nucleophile. The both species are partially bonded to opposite sides of the carbon atom in the transition state.

Recall that an SN2 reaction is driven by the attraction between the negative charge of the nucleophile (OH^-) and the positive charge of the electrophile (the partial positive charge on the carbon atom bearing the chlorine leaving group).

4 0
3 years ago
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