<span>Evaporation is the process of atoms or molecules in a liquid, or solid state (depending on the state of the substance sublimes) gains enough energy to become gaseous. </span>
V(C₄H₆O₃) = 5.00 mL.
d(C₄H₆O₃) = 1.08 g/mL.
m(C₄H₆O₃) = V(C₄H₆O₃) · d(C₄H₆O₃).
m(C₄H₆O₃) = 5.00 mL · 1.08 g/mL.
m(C₄H₆O₃) = 5.4 g.
n(C₄H₆O₃) = m(C₄H₆O₃) ÷ M(C₄H₆O₃).
n(C₄H₆O₃) = 5.4 g ÷ 102 g/mol.
n(C₄H₆O₃) = 0.0529 mol.
n(C₇H₆O₃) = 2.08 g ÷ 138.1 g/mol.
n(C₇H₆O₃) = 0.015 mol; limiting reactant.
From chemical reaction: n(C₄H₆O₃) : n(C₉H₈O₄) = 1 : 1.
n(C₉H₈O₄) = 0.015 mol.
m(C₉H₈O₄) = 0.015 mol · 180.16 g/mol.
m(C₉H₈O₄) = 2.71 g; theoretical yield.
percent yield od aspirine = 2.57 g ÷ 2.71 g · 100% = 94.83%.
Answer: The factor that lead to cyclopropane being less stable than the other cycloalkanes is the presence of a RING STRAIN.
Explanation:
In organic chemistry, the end carbon atoms of an open aliphatic chain can join together to form a closed system or ring to form cycloalkanes. Such compounds are known as cyclic compounds. Examples include cyclopropane, cyclobutane, cyclopentane and many among others.
Cyclopropane is less stable than other cycloalkanes mentioned above because of the presence of ring strain in its structural arrangement. The ring strain is the spatial orientation of atoms of the cycloalkane compounds which tend to give off a very high and non favourable energy. The release of heat energy which is stored in the bonds and molecules cause the ring to be UNSTABLE and REACTIVE.
The presence of the ring strain affects mainly the structures and the conformational function of the smaller cycloalkanes. cyclopropane, which is the smallest cycloalkane than the rest mentioned above, contains only 3 carbons with a small ring.
109/8.56=12.7
50+12.7
V=62.7
Mass= Volume x Density so i divided the mass and density to get the volume. and afterwards i would just add it to the mass to get my final answer
Your answer is C. Both gasoline and litter would need to be physically separated from the water, because neither bonds with the water.
