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.
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Answer:The molar mass of atoms of an element is given by the standard relative atomic mass of the element multiplied by the molar mass constant, 1 × 10−3 kg/mol = 1 g/mol.
Explanation:
Answer: 12.18 u
Explanation: The average atomic mass of an element is calculated by taking the weighted average of the atomic masses of its stable isotopes.
In other words, each stable isotope will contribute to the average mass of the element proportionally to its abundance.
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