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Write the structure of the major organic product expected from each of the following reaction phenol and Na OH?
The following reaction needs to be given for someone to know how to write the structure of the major organic product expected from it. With this not being given a person will not know how to write the structure.
Is the SO3H group activating or deactivating in the given reaction?
In the given reaction, the SO3H group is activating.
What kind of reaction -SN1 or SN2 or E1 or E2- is expected for secondary haloalkanes with sterically hindered strong bases?
E2 reaction is expected for secondary haloalkanes with sterically hindered strong bases. This is because the strong base can readily abstract a proton from the beta position, leading to the elimination of the leaving group and formation of the alkene product.
Will acetaldehyde give positive haloform reaction?
Yes. The alpha protons on the methyl group will be deprotonated and react with halides and eventually form a trihaloform group or (-C-CX3). The Trihalofrom is explelled when a OH group attacks the carbonyl carbon. This forms the trihaloform carbanion of the carboxylic acid. The anion takes a hydrogen from the acid to form the haloform and a carboxylic salt
What makes a leaving group good in a chemical reaction?
A leaving group is considered good in a chemical reaction if it can easily detach from the molecule, allowing the reaction to proceed efficiently. This is typically achieved when the leaving group is stable and can form a stable product after leaving the molecule.
What is heats in swimming?
A heat in swimming is like a group of swimmers swimming the same event. Since only a certain number of swimmers can swim at a time (depending on the number of lanes, usually 8) they have to have swim at different times and usually they place heats on how fast they swim. So, if you have the fastest time going into the race then you'd be in the last heat and if you have the slowest time going into the race then you'd be in the first heat. Also they place you in lanes from slowest to fastest (if you have the fastest time you go in the 4th lane and slowest goes in the outer lanes). Hope this helps. Source: Many years of competitive swimming
Write the structure of the major organic product expected from each of the following reaction phenol and Na OH?
The following reaction needs to be given for someone to know how to write the structure of the major organic product expected from it. With this not being given a person will not know how to write the structure.
Is the SO3H group activating or deactivating in the given reaction?
In the given reaction, the SO3H group is activating.
What kind of reaction -SN1 or SN2 or E1 or E2- is expected for secondary haloalkanes with sterically hindered strong bases?
E2 reaction is expected for secondary haloalkanes with sterically hindered strong bases. This is because the strong base can readily abstract a proton from the beta position, leading to the elimination of the leaving group and formation of the alkene product.
Will acetaldehyde give positive haloform reaction?
Yes. The alpha protons on the methyl group will be deprotonated and react with halides and eventually form a trihaloform group or (-C-CX3). The Trihalofrom is explelled when a OH group attacks the carbonyl carbon. This forms the trihaloform carbanion of the carboxylic acid. The anion takes a hydrogen from the acid to form the haloform and a carboxylic salt
What is the expected number of valence electrons for a group 3 A element?
The expected number of valence electrons for a group 3A element is 3. These elements have three valence electrons because they are located in group 3A of the periodic table, which corresponds to the third column from the left.
What is the same between the experimental and control group?
The similarity between the experimental group and the control group is that in both cases, results are expected.
Which group on the periodic table will gain an electron in reaction?
group 17 - the halogens
What makes a leaving group good in a chemical reaction?
A leaving group is considered good in a chemical reaction if it can easily detach from the molecule, allowing the reaction to proceed efficiently. This is typically achieved when the leaving group is stable and can form a stable product after leaving the molecule.
What do the initials of the R and B group Next stand for?
Never EXpecTed
What makes a leaving group the best choice in a chemical reaction?
A leaving group is the best choice in a chemical reaction because it can easily detach from the molecule, allowing the reaction to proceed efficiently. The leaving group's ability to stabilize negative charge and leave the molecule helps in forming new bonds and driving the reaction forward.
How does potassium behave during a chemical reaction?
Group I cations are typically spectator ions in a reaction
