Electron Push and Pull: Inductive Effects Explained

The video tutorial explains the concept of inductive effects in organic chemistry, focusing on the minus I effect, where electronegative groups withdraw electrons, and the plus I effect, where electron-donating groups release electrons. It discusses the characteristics and order of these effects, highlighting that the minus I effect generally dominates when both effects are present in a compound, as illustrated with the example of 2-chloropropane.

How do the minus I and plus I effects interact when both are present in the same carbon chain?

Provide an example of a compound where the minus I effect dominates and explain why.