Why are aromatic compounds such as toluene and oxygenated hydrocarbons such as ethanol generally used as antiknock agents?
Simply because they work.
When filling up your car with gasoline, different brands will tout different additives; most formulations would be very similar. The addition of certain additives to your hydrocarbon mix results in better performance in your combustion engine. This is the domain of an engineer, not a chemist.
By signing up, you agree to our Terms of Service and Privacy Policy
Aromatic compounds like toluene and oxygenated hydrocarbons like ethanol are used as antiknock agents because they have high octane ratings, which means they resist detonation or knocking in internal combustion engines. They have a slower combustion rate compared to straight-chain hydrocarbons, allowing for more controlled and efficient combustion in the engine, thus reducing knocking and engine damage.
By signing up, you agree to our Terms of Service and Privacy Policy
When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.
When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.
When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.
When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.
- What do the functional groups determine?
- Why are functional groups important?
- What makes a cycloalkane different from other alkanes?
- How can I draw the following ethers: 1-propoxypentane, 2-ethoxybutane, 1-methoxy-4-chlorohexane, and 3-butoxy-2,4-dimethyloctane?
- What is the mechanism of the reaction of NaI in acetone with an alkyl halide?
- 98% accuracy study help
- Covers math, physics, chemistry, biology, and more
- Step-by-step, in-depth guides
- Readily available 24/7