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3 years ago

Caculate the kinetic energy in J of an electron moving at 6.00x 10 to the sixth power m/s.

Chemistry

1 answer:

asambeis [7]3 years ago

5 0

Answer:

$1.64x10^-^1^7 J$

Explanation:

Due to you know the velocity of the electron, the only thing that you need to do is used the Newtonian kinetic energy formula. The kinetic energy is defined as the work needed by motion body of a given mass to accelerate from rest to its know velocity:

$KE=1/2mv^2=[kg*(m/s)^2]=[J]$

$m_e_- =9.1093835x10^-^3^1 kg$

$KE=9.11x10^-^3^1 kg*(6.00x10^6 m/s)^2=1.64x10^-^1^7 J$

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How manymoles of each ion are present in 175 mL of 0.147 M Fe2(SO4)3?

lilavasa [31]

Answer: 0.0257 moles of $Fe^{3+}$ and 0.0257 moles of $SO_4^{2-}$

Explanation:

Molarity of a solution is defined as the number of moles of solute dissolved per Liter of the solution.

$Molarity=\frac{moles}{\text {Volume in L}}$

moles of $Fe_2(SO_4)_3=Molarity\times {\text {Volume in L}}=0.147\times 0.175L=0.0257moles$

The balanced reaction for dissociation will be:

$Fe_2(SO_4)_3\rightarrow Fe^{3+}+SO_4^{2-}$

According to stoichiometry:

1 mole of $Fe_2(SO_4)_3$ gives 1 mole of $Fe^{3+}$ and 1 mole of $SO_4^{2-}$

Thus there will be 0.0257 moles of $Fe^{3+}$ and 0.0257 moles of $SO_4^{2-}$

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3 years ago

How do scientist communicate the results of an investigation?

maks197457 [2]

Answer:

scientists often communicate their research results in three general ways:

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2) Two is to present their results at national and international conferences where other scientists can listen to presentations

Explanation:

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3 years ago

Read 2 more answers

Draw the structure(s) of the major organic product(s) of the following reaction. 1. lithium diisopropylamide / hexane 2. 1 eq. C

Jobisdone [24]

Answer:

See explanation below

Explanation:

You are not providing the starting material, however, I manage to find a similar question to this, so I'm gonna use it as a basis to help you answer yours.

Now let's analyze what is happening in the reaction so we can predict the final product.

We have a ketone here, reacting at first with LDA. This is a very strong base that is commonly used in reactions with ketones and aldehydes to promove a condensation. To do this, as LDA is a strong base it will occur firts an acid base reaction, substracting the most acidic hydrogen in the molecule (Which in this case, is the Beta hydrogen of the carbonile). This will cause an enolate formation.

Then, this enolate will react with the CH3I and form a new product. The final result would be a ketone with a methyl group now attached. In the picture 2, you have the mechanism and final product.

Hope this helps