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EleoNora [17]
3 years ago
14

What can be done to remove a magnetic force around an electromagnet

Chemistry
1 answer:
Harrizon [31]3 years ago
7 0
D is to stop the current and the force can be removed
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What is the formula for silicon tetrabromide?
bogdanovich [222]

Answer:

SiBr4

Explanation:

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One method used commercially to peel potatoes is to soak them in a solution of NaOH for a short time and then remove them from t
sergij07 [2.7K]

Answer:

b. 2.28 M

Explanation:

The reaction of neutralization of NaOH with H2SO4 is:

2NaOH + H2SO4 → Na2SO4 + 2H2O

<em>Where 2 moles of NaOH react per mole of H2SO4</em>

<em />

To solve the concentration of NaOH we need to find the moles of H2SO4. Using the chemical equation we can find the moles of NaOH that react and with the volume the molar concentration as follows:

<em>Moles H2SO4:</em>

45.7mL = 0.0457L * (0.500mol/L) = 0.02285 moles H2SO4

<em>Moles NaOH:</em>

0.02285 moles H2SO4 * (2moles NaOH / 1 mol H2SO4) = 0.0457moles NaOH

<em>Molarity NaOH:</em>

0.0457moles NaOH / 0.020L =

2.28M

Right option:

<h3>b. 2.28 M</h3>
7 0
2 years ago
Which of the following is used in pencils?
Mamont248 [21]

Answer:

1st answer:  A. Graphite

2nd answer:  B.  Mercury

Explanation:

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Which statement correctly contrasts science and pseudoscience
mojhsa [17]
brainly.com/question/1470976 Hope this helps!
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Explain what a glycosolation reaction is
AVprozaik [17]

Answer:

The glycosylation reaction or glycoside formation is an organic reaction in which the hemiacetal group of cyclists ketoses or aldoses turns into acetals, named glycosides. Reaction in the attached picture.

Explanation:

Carbohydrates can be found in an open-chain form or a cyclic form. For the second one, the carbonyl group of the aldehyde could react with the alcohol group of the molecule to form the cycle. As shown in the attached picture, the alcohol group of this cyclic form could react with an alcohol (like methanol) in acidic conditions to form an acetal. These compounds are stable at neutral and acidic conditions, but they hydrolyze at basic conditions. This reaction produces both acetals anomers (α and β) because the attack of the nucleophile (alcohol) could be from both sides. However, the most stable anomer will predominate.

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3 years ago
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