What is the synthesis of ferrocene?
Industrial synthesis Industrially, ferrocene is synthesized by the reaction of iron(II) ethoxide with cyclopentadiene; the iron(II) ethoxide needed is produced by the electrochemical oxidation of metallic iron in anhydrous ethanol.
What is the formula of ferrocene?
C10H10FeFerrocene / Formula
Which of the following reaction are shown by ferrocene?
Hence, the reactions shown by benzene, due to aromatic character, are also exhibited by ferrocene. Ferrocene is represented in the following reactions as Fe(η5-C5H5)2/Fe(Cp)2. Ferrocene has found two interesting applications related to fuel. It is known to promote the smoke-free combustion of fuel.
Which of the following statement is correct for the ferrocene?
D. Ferrocene is an organometallic compound.
What reactions can ferrocene undergo?
Ferrocene will undergo alkylation, acylation, sulphonation, metalation, arylation, formylation, amino- methylation, arid other reactions characteristic of a highly reactive aromatic system.
What is the oxidation state of iron in ferrocene?
+2
Let the oxidation state of Fe be x, and in ferrocene, there are 2 cyclopentadienyl ligands in which each ligand have a negative charge Therefore x+(-1×2)=0, this implies x=+2. Hence the oxidation state is +2.
What is the Iupac name of ferrocene?
ferrocene, bis(η5-cyclopentadienyl)ironFerrocene / IUPAC ID
Which of the following statement is incorrect about ferrocene?
1. Which of the following statement is not true about ferrocene? Explanation: Cyclopentadienyl ring in ferrocene are staggered is a wrong statement.
Which of the following is not considered as an organometallic compound?
Grignard reagent: The chemical formula of Grignard reagent is R−MgX where Mg is a metal and R is any organic group. Hence, it is an organometallic compound. Therefore, the correct option is option B because cis-platin does not obey the criteria to be called an organometallic compound.
Why does ferrocene undergo electrophilic substitution reaction?
Due to the aromatic character of the cyclopentadienyl ligands, ferrocene can undergo electrophilic aromatic substitution reactions typical of aromatic compounds such as benzene.
How do you find the oxidation state of ferrocene?
Let the oxidation state of Fe be x, and in ferrocene, there are 2 cyclopentadienyl ligands in which each ligand have a negative charge Therefore x+(-1×2)=0, this implies x=+2. Hence the oxidation state is +2.
Which of the following reaction is not given by ferrocene?
2. Ferrocene cannot undergo which of the following reaction? Explanation: Ferrocene cannot undergo Diels-Alder reaction because it does not satisfy requirements of Diels-Alder reaction (dienophile).