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Questions and Answers
What acid can be used as a catalyst in Friedel Craft’s catalyst reaction?
What acid can be used as a catalyst in Friedel Craft’s catalyst reaction?
Amongst the following, which compound can be most readily sulphonated?
Amongst the following, which compound can be most readily sulphonated?
What type of reaction can benzene not undergo?
What type of reaction can benzene not undergo?
Which group below is considered to have a deactivating effect during substitution?
Which group below is considered to have a deactivating effect during substitution?
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Which substitution present on the benzene ring would not lead to meta orientation with deactivation?
Which substitution present on the benzene ring would not lead to meta orientation with deactivation?
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What is the process of acylation of benzene to produce aliphatic aromatic ketones known as?
What is the process of acylation of benzene to produce aliphatic aromatic ketones known as?
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What is the bond angle in benzene (in degrees)?
What is the bond angle in benzene (in degrees)?
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Ozonolysis of benzene gives:
Ozonolysis of benzene gives:
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What is the bond length in benzene between carbon atoms (in Angstroms)?
What is the bond length in benzene between carbon atoms (in Angstroms)?
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What is the hybridization in benzene?
What is the hybridization in benzene?
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Which property is characteristic of benzene?
Which property is characteristic of benzene?
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Which characteristics are characteristic of aromatic compounds?
Which characteristics are characteristic of aromatic compounds?
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Cyclopentadienyl anion and cyclopropenyl anion are...
Cyclopentadienyl anion and cyclopropenyl anion are...
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Which of the following substances has delocalized electrons?
Which of the following substances has delocalized electrons?
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What type of bonds indicate the presence of hydrogen and halogen addition reactions in benzene?
What type of bonds indicate the presence of hydrogen and halogen addition reactions in benzene?
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What is the heat of hydrogenation of cyclohexane (in kJ/mol)?
What is the heat of hydrogenation of cyclohexane (in kJ/mol)?
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