Valence electrons are the electrons in the outermost shell. Those are t<span>he electrons on an atom that can be gained or lost in a chemical reaction.
</span>Elements that are left on the periodic table <span> have relatively few </span>valence electrons<span>, and can form ions more easily by losing their </span>valence electrons<span> to form positively charged cations.</span>
<span>Nonmetals are further to the right on the periodic table, so they gain electrons relatively easily and lose them with difficulty. </span>
Answer:
MgSO4.7H2O
Explanation:
Let the formula for the hydrated magnesium sulphate be MgSO4.xH2O
Mass of the hydrated salt (MgSO4.xH2O) = 12.845g
Mass of anhydrous salt (MgSO4) = 6.273g
Mass of water molecule(xH2O) = Mass of the hydrated salt — Mass of anhydrous salt = 12.845 — 6.273 = 6.572g
Now,we can obtain the number of mole of water molecule present in the hydrated salt as follows:
Molar Mass of hydrated salt (MgSO4.xH2O) = 24 + 32 + (16x4) + x(2 + 16) = 24 + 32 + 64 + x(18) = 120 + 18x
Mass of xH2O/ Molar Mass of MgSO4.xH2O = Mass of water / mass of hydrated salt
18x/120 + 18x = 6.572/12.845
Cross multiply to express in linear form
18x x 12.845 = 6.572(120 + 18x)
231.21x = 788.64 + 118.296x
Collect like terms
231.21x — 118.296x = 788.64
112.914x = 788.64
Divide both side by 112.914
x = 788.64 /112.914
x = 7
Therefore the formula for the hydrated salt (MgSO4.xH2O) is MgSO4.7H2O
Bohrs model says that electrons move in fixed shells (which have fixed distances) around the nucleus of an atom.
Resonance, leaving group, carbonyl carbon delta+, and steric effect is the most crucial variables that affect the relative reactivity of a functional group containing a carbonyl in an addition or substitution process.
Discussion:
1. Carbonyl Carbon Delta+: The carbonyl group becomes more electrophilic and accelerates nucleophilic assault when the carbonyl carbon delta+ is bigger.
2. Resonance: When the carbonyl is transformed into the tetrahedral adduct, it may be lost. Loss of resonance increases the energy of the transition state for this nucleophilic assault because resonance has the function of stabilizing. Therefore, a carbonyl functional group's resistance to nucleophilic attack increases as resonance in the group increases in importance.
3. Leaving group: Tetrahedral adduct fragmentation is encouraged by a better LG.
4. Steric effects: The nucleophilic attack on carbonyl carbon is delayed when sterically impeded.
Learn more about carbonyl here:
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