Two protons and two neutrons are emitted and trapped as materials like uranium and thorium deep underground decay into radium and thorium, respectively. These alpha-particles transform into stable helium atoms as they take on electrons from their surroundings.
<h3>
What elements go through alpha decay?</h3>
Alpha decay usually occurs in heavy nuclei such as uranium or plutonium, and therefore is a major part of the radioactive fallout from a nuclear explosion.
<h3>
Where does alpha decay occur?</h3>
Alpha decay occurs most often in massive nuclei that have too large a proton to neutron ratio. An alpha particle, with its two protons and two neutrons, is a very stable configuration of particles.
Learn more about alpha decay here:
brainly.com/question/1898040
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Answer:
Explanation:
This is a limiting reactant problem.
Mg(s)
+
2HCl(aq)
→
MgCl
2
(
aq
)
+ H
2
(
g
)
Determine Moles of Magnesium
Divide the given mass of magnesium by its molar mass (atomic weight on periodic table in g/mol).
4.86
g Mg
×
1
mol Mg
24.3050
g Mg
=
0.200 mol Mg
Determine Moles of 2M Hydrochloric Acid
Convert
100 cm
3
to
100 mL
and then to
0.1 L
.
1 dm
3
=
1 L
Convert
2.00 mol/dm
3
to
2.00 mol/L
Multiply
0.1
L
times
2.00 mol/L
.
100
cm
3
×
1
mL
1
cm
3
×
1
L
1000
mL
=
0.1 L HCl
2.00 mol/dm
3
=
2.00 mol/L
0.1
L
×
2.00
mol
1
L
=
0.200 mol HCl
Multiply the moles of each reactant times the appropriate mole ratio from the balanced equation. Then multiply times the molar mass of hydrogen gas,
2.01588 g/mol
0.200
mol Mg
×
1
mol H
2
1
mol Mg
×
2.01588
g H
2
1
mol H
2
=
0.403 g H
2
0.200
mol HCl
×
1
mol H
2
2
mol HCl
×
2.01588
g H
2
1
mol H
2
=
0.202 g H
2
The limiting reactant is
HCl
, which will produce
0.202 g H
2
under the stated conditions.
pls mark as brainliest ans
Hydrochloric acid + Sodium hydroxide =Sodium chloride +water
False because particles stop moving or study slow down.
<h3><u>Full Question:</u></h3>
The following compound has been found effective in treating pain and inflammation (J. Med. Chem. 2007, 4222). Which sequence correctly ranks each carbonyl group in order of increasing reactivity toward nucleophilic addition?
A) 1 < 2 < 3
B) 2 < 3 < 1
C) 3 < 1 < 2
D) 1 < 3 < 2
<h3><u>Answer: </u></h3>
The rate of nucleophilic attack of carbonyl compounds is 2<3 <1.
Option B
<h3><u>Explanation. </u></h3>
Nucleophilic attack is explained as the attack of an electron rich radical to a carbonyl compound like aldehyde or a ketone. A nucleophile has a high electron density, so it searches for a electropositive atom where it can donate a portion of its electron density and become stable.
A carbonyl compound is a 
hybridized carbon atom with a double bonded oxygen atom in it. The oxygen atom pulls a huge portion of electron density from carbon being very electropositive.
In a ketone, there are two factors that make it less likely to undergo a nucleophilic attack than aldehyde. Firstly, the steric hindrance of two carbon groups being attached with the carbonyl carbon makes it harder for the nucleophile to approach. Secondly, the electron push by the carbon groups attached makes the carbonyl carbon a bit less electropositive than the aldehyde one. So aldehydes are more reactive towards a nucleophilic addition reaction.
