key term - Steric Hindrance

Definition

Steric hindrance, also known as steric strain or steric effect, refers to the repulsive forces that arise between atoms or groups of atoms in a molecule due to their physical size and spatial arrangement. This phenomenon can significantly impact the stability, reactivity, and conformations of organic compounds.

5 Must Know Facts For Your Next Test

1. Steric hindrance can influence the stability and reactivity of organic compounds by favoring certain conformations over others.
2. In the context of alkane conformations, steric hindrance between bulky substituents, such as methyl groups, can lead to the preference for the staggered conformation over the eclipsed conformation.
3. Steric effects play a crucial role in the stability of cycloalkanes, with smaller ring sizes experiencing greater ring strain due to the inability of the atoms to adopt their preferred bond angles.
4. Steric hindrance can impact the stereochemistry of organic reactions, such as the SN2 mechanism, where the approach of the nucleophile can be hindered by the presence of bulky substituents.
5. The basicity of amines can be affected by steric hindrance, as the bulky substituents can impede the approach of protons or other electrophiles to the nitrogen atom.

Review Questions

• Explain how steric hindrance influences the conformations of ethane and other alkanes.
  • Steric hindrance plays a crucial role in determining the preferred conformations of ethane and other alkanes. In ethane, the two methyl groups experience repulsive forces when in the eclipsed conformation, leading to a higher potential energy and less stability. To minimize this steric strain, ethane and other alkanes prefer to adopt the staggered conformation, where the methyl groups are oriented as far apart as possible. This preference for the staggered conformation is observed across alkanes of varying chain lengths, as the minimization of steric hindrance between bulky substituents is a key factor in determining the most stable conformations.
• Describe the impact of steric hindrance on the stability and reactivity of cycloalkanes.
  • Steric hindrance significantly affects the stability and reactivity of cycloalkanes. In smaller ring sizes, such as cyclopropane and cyclobutane, the atoms are forced to adopt bond angles that deviate from the ideal tetrahedral arrangement, leading to increased torsional and angle strain. This steric strain destabilizes the cycloalkane and makes it more reactive compared to acyclic alkanes. As the ring size increases, the atoms can adopt more favorable bond angles, and the steric strain is reduced, leading to greater stability. The conformational flexibility of larger cycloalkanes, such as cyclohexane, is also influenced by steric effects, with the chair conformation being the most stable due to the minimization of 1,3-diaxial interactions.
• Analyze the role of steric hindrance in determining the stereochemistry and reactivity of the SN2 reaction.
  • Steric hindrance plays a critical role in the stereochemistry and reactivity of the SN2 (nucleophilic substitution, bimolecular) reaction. In the SN2 mechanism, the incoming nucleophile attacks the carbon bearing the leaving group from the opposite side, resulting in the inversion of configuration at the stereogenic center. However, the presence of bulky substituents around the carbon can hinder the approach of the nucleophile, making the SN2 reaction less favorable. Smaller, less sterically hindered substrates are more reactive in SN2 reactions, as the nucleophile can more easily access the carbon center and displace the leaving group. Conversely, substrates with larger, more bulky substituents are less reactive in SN2 reactions due to the increased steric hindrance, which can lead to the preference for alternative reaction pathways, such as the SN1 mechanism.

Related terms

Van der Waals Radius: The van der Waals radius is the effective size of an atom or molecule, including the surrounding electron cloud, which determines the minimum distance of approach between two atoms or molecules.

Torsional Strain:

Torsional strain, or angle strain, is the strain that arises when atoms or groups are forced to adopt a less favorable dihedral angle, leading to increased potential energy in the molecule.

Conformational Analysis:

Conformational analysis is the study of the various three-dimensional arrangements that a molecule can adopt, taking into account factors such as bond lengths, bond angles, and steric effects.