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What is the mechanism for the addition of bromine to an alkene?
The mechanism for the addition of bromine to an alkene involves the formation of a bromonium ion intermediate, which is then attacked by a bromide ion to yield a dihalide product. This process is known as electrophilic addition.
Write equations that illustrate the mechanism of the basic hydrolysis of benzonitrile to benzoate ion?
The basic hydrolysis of benzonitrile to benzoate ion involves the reaction with hydroxide ions (OH-) to form benzoate ion. The mechanism can be represented as: Benzonitrile + OH- → Benzonitrile-OH Benzonitrile-OH + OH- → Benzoate ion + H2O
What is the reaction mechanism for the addition of chlorine to cyclohexene in the presence of Cl2?
The reaction mechanism for the addition of chlorine to cyclohexene in the presence of Cl2 involves the formation of a cyclic halonium ion intermediate, followed by nucleophilic attack by chloride ion to form a dihalogenated product.
Which of these is not a subatomic particle proton ion neutron or electron?
Ion.
What is the reaction mechanism for the addition of HBr to 1,3-pentadiene?
The reaction mechanism for the addition of HBr to 1,3-pentadiene involves the formation of a carbocation intermediate followed by the attack of the bromide ion to form the final product.
What is the reaction mechanism for the addition of HBr to 2,4-hexadiene?
The reaction mechanism for the addition of HBr to 2,4-hexadiene involves the formation of a carbocation intermediate followed by the attack of the bromide ion to form the final product.
Write an equation that shows the formation of a sodium ion from a neutral sodium atom.?
Na -> Na+ + e-
How can a charged atom attract a neutron?
A neutron has no charge, so a charged atom (ion) cannot attract a neutron.
Which has less electric charge ion electron neutron or proton?
A neutron, which has neutral charge
Give a reaction mechanism for iodoform reaction using propanone?
In the iodoform reaction using propanone, the methyl ketone group of propanone undergoes halogenation and substitution reactions with iodine and sodium hydroxide. The mechanism involves formation of the enolate ion, followed by a nucleophilic attack of the iodine ion to yield iodoform as the final product.
What is the mechanism of the sodium borohydride reaction with methanol?
The mechanism of the sodium borohydride reaction with methanol involves the transfer of a hydride ion from sodium borohydride to methanol, resulting in the formation of sodium methoxide and hydrogen gas. This reaction is a nucleophilic addition-elimination process, where the hydride ion acts as a nucleophile attacking the electrophilic carbon in methanol.
What is the suffix for formation?
ion
