The reaction rate of the SN1 reaction change if the electrophile is switched from the tertiary electrophile to a secondary electrophile will decrease.
SN1 exhibits substitution, nucleophilicity, and monomolecular reaction, and is expressed by the expression rate = k [R-LG]. This means that the rate-determining step of the mechanism depends on the degradation of a single molecular species. Multi-step reactions include intermediates and multiple transition states (TS).
The SN1 reaction is a nucleophilic substitution reaction in which the nucleophile replaces the leaving group (similar to SN2). However, the SN1 reaction is a single molecule. The rate of this reaction depends on the concentration of only one reactant.
Learn more about reaction rate here: brainly.com/question/7578129
#SPJ4
The formula for potassium sulfide is K2S
1. A radical is a reactive intermediate with a single ____________ electron, formed by ____________ of a covalent bond.
1. A: Unpaired, and homolysis
2. Allylic radicals are stabilized by ____________ , making them ____________ stable than tertiary radicals.
2. A: Resonance, and more
3. A compound that contains an especially weak bond that serves as a source of radicals is called a radical ____________ .
3. A: Initiator
4. Treatment of cyclohexene with N-bromosuccinimide in the presence of light leads to ____________ by ____________ intermediates.
4. A: Allylic substitution by radical
There are some methods that differentiate waves; one thing is by its medium.
Electromagnetic waves did not require a medium for transmission such as in a
vacuum while mechanical waves require a medium to travel such as air, water or
anything that can serve as a transmission aid.
The most common sample of EM waves in
telecommunication is radio,
light and infra-red signals. An example of a mechanical wave is a sound
wave, which requires air to travel. Oscillating molecules made the
sound waves.
Answer:
Number of Significant Figures: 5
The Significant Figures are 1 1 0 0 5
Explanation:
