Answer:
A molecule is tetrahedral if the central atom has four bonds and no lone pairs.
Explanation:
A typical example is a molecule of methane (see image).
The electron pairs in the bonds repel the electrons in the other bonds, so they all try to get as far from each other as possible.
They can do this if the bonds point to the corners of a tetrahedron, with bond angles of 109.5°.
<span>The correct answer is 3: 0.10 M K3PO4(aq). The higher the concentration (or molarity), the higher the boiling point. Thus, the solution with the most moles will have the highest boiling point. SO4, PO4, and NO3 are all polyatomic ions, so by definition, they only have one mole. In K3PO4, K3 has 3 moles and PO4 has 1 mole, meaning all together it has 4 moles (more than any of the other options).</span>
Answer:
I'd Go. B. weigh everything, let the reaction happen, then weigh everything again.
<span>Answer: 17.8 cm
</span>
<span>Explanation:
</span>
<span>1) Since temperature is constant, you use Boyle's law:
</span>
<span>PV = constant => P₁V₁ = P₂V₂
</span><span>=> V₁/V₂ = P₂/P₁</span>
<span>
2) Since the ballon is spherical:
</span><span>V = (4/3)π(r)³</span>
<span>
Therefore, V₁/V₂ = (r₁)³ / (r₂)³
</span>
<span>3) Replacing in the equation V₁/V₂ = P₂/P₁:
</span><span><span>(r₁)³ / (r₂)³ </span>= P₂/P₁</span>
<span>
And you can solve for r₂: (r₂)³ = (P₁/P₂) x (r₁)³
</span>(r₂)³ = (1.0 atm / 0.87 atm) x (17 cm)³ = 5,647.13 cm³
<span>
r₂ = 17.8 cm</span>
Benzaldehyde or C6H5CHO would not undergo the aldol condensation because it does not contain an alpha-hydrogen in its structure. Aldol condensation is a type of reaction that happens between an enolate and an aldehyde or ketone leading to a alkene that has a planar structure. The lack of an alpha-hydrogen would not allow for it to undergo such process since it cannot enolize. Benzaldehyde undergoes a nucleophilic reaction known as Claisen-Schmidt condensation. It has somehow same mechanism of the aldol reaction however, the nucleophilic attack on the carbonyl happens even without the alpha-hydrogen but with an enolate that is from a ketone.