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What else can I help you with?
Do rearrangements occur in E1 reactions?
carbocation is formed as an intermediate so rearrangement is possible
What reactions is possible according to Dalton's atomic theory?
According to Dalton's atomic theory, reactions involve the rearrangement of atoms to form new compounds, but atoms themselves are not created or destroyed during a chemical reaction. This theory also states that atoms combine in simple ratios to form compounds.
Why do you get isopropyl benzene on treating benzene with 1 - chloropropane instead of n - propyl benzene?
Isopropylbenzene forms when treating benzene with 1-chloropropane instead of n-propylbenzene because 1-chloropropane undergoes an S N 1 mechanism due to the carbocation intermediate formed. This leads to rearrangement of the carbocation to a more stable secondary carbocation, favoring the formation of isopropylbenzene over n-propylbenzene.
Why are substitutions at 4' and 6' positions of 3-chloro toluene not normally possible?
Substitutions at 4' and 6' positions of 3-chloro toluene are not normally possible because carbocations are prone to rearrangement.
Is plutonium oxidizing?
Plutonium is easily oxidized: plutonium oxides are PuO2, PuO; intermediate oxides are possible.
Do rearrangements occur in E1 reactions?
carbocation is formed as an intermediate so rearrangement is possible
When two atoms combine to form a largest atom?
It is possible by the intermediate of nuclear reactions at high energy - see the preparation of the transfermium artificial chemical elements.
What reactions is possible according to Dalton's atomic theory?
According to Dalton's atomic theory, reactions involve the rearrangement of atoms to form new compounds, but atoms themselves are not created or destroyed during a chemical reaction. This theory also states that atoms combine in simple ratios to form compounds.
Is CCl4 to CH4 possible according to Dalton's theory?
According to Dalton's theory, chemical reactions involve the rearrangement of atoms and do not create or destroy atoms. Therefore, the transformation of CCl4 to CH4 would not be possible as it involves the addition of hydrogen atoms and the removal of chlorine atoms, which violates the law of conservation of atoms.
Is it possible for an alkyl halide to undergo sn1 and also sn2 reactions?
Yes an alkyl halide can undergo both Sn1 and Sn2 reactions - it just depends on what kind of alkyl halide it is. Methyl halides such as CH3Br/CH3Cl/CH3I, etc. are most suitable for Sn2 reactions because they are less sterically hindered by R-groups (they are not "bulky"). This allows for easy attack by the nucleophile. Primary alkyl halides (RCH2X) are also most suitable for Sn2 because of the same reason above Secondary alkyl halides can undergo both Sn1 and Sn2 reactions, this depends on other factors such as solvent and leaving group and nucleophile. If the solvent is polar aprotic, the reaction will go Sn2, if polar protic - Sn1. Tertiary alkyl halides (alkyl halides with 4 r-groups) do not go Sn2 because they are bulky and the R-groups stabilize the carbocation by hyperconjugation and inductive effect.
Why do you get isopropyl benzene on treating benzene with 1 - chloropropane instead of n - propyl benzene?
Isopropylbenzene forms when treating benzene with 1-chloropropane instead of n-propylbenzene because 1-chloropropane undergoes an S N 1 mechanism due to the carbocation intermediate formed. This leads to rearrangement of the carbocation to a more stable secondary carbocation, favoring the formation of isopropylbenzene over n-propylbenzene.
Why are substitutions at 4' and 6' positions of 3-chloro toluene not normally possible?
Substitutions at 4' and 6' positions of 3-chloro toluene are not normally possible because carbocations are prone to rearrangement.
How do you cut a diamond with your fist?
This action is probably not possible without intermediate tools, such as a wedge and a hammer.
What is One step in a series of steps that take place in a chemical change?
A possible step in a chemical change process is the breaking of chemical bonds in reactant molecules to form intermediate species. This step is often followed by the rearrangement of atoms to form new bonds and ultimately the creation of one or more products.
Is it possible after car accident have a late reactions?
yes
What are the possible dangers if the intermediate shaft is not repaired soon?
It will fly out in a violent fashion causing a mayhem. Seriously.
Is plutonium oxidizing?
Plutonium is easily oxidized: plutonium oxides are PuO2, PuO; intermediate oxides are possible.
