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.
<u>Answer:</u>
Earth's axis and position around the sun.
<u>Explanation:</u>
Earth's tilted axis causes the seasons to change. Throughout the year, different parts of Earth acquire the Sun's most direct rays(Or heat) because of the orbital rotation of Earth. So, when the North Pole tilts toward the Sun, it's summer inside the Northern Hemisphere. And whilst the South Pole tilts towards the Sun, it is winter within the Northern Hemisphere and vise versa.
Answer:
Carbon 3 is double bonded to an oxygen and attached to carbon 2 and carbon 4. :
Answer: Carbonyl group ( Ketone or aldehyde)
Carbon 17 is attached to an oxygen, which is attached to a hydrogen. :
Answer: Carboxyl group (Carboxylic acid)
A central carbon is attached to an amine, two hydrogens, and a carbon that is double bonded to an oxygen and single bonded to an oxygen attached to a hydrogen. :
Answer: Amide group
An amide group contains both amine and carboxyl
