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Out of aniline and N-nitrosoamine..........

Out of aniline and N-nitrosoamine........is carcinogenic

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To determine which compound is carcinogenic between aniline and N-nitrosamine, we can follow these steps: ### Step 1: Define the Compounds - **Aniline**: Aniline is an organic compound with the formula C6H5NH2. It consists of a benzene ring attached to an amino group (-NH2). - **N-nitrosamine**: N-nitrosamines are a class of compounds that contain a nitroso group (N=O) attached to a nitrogen atom that is also bonded to an alkyl or aryl group. The general structure can be represented as R-N(NO)-R', where R and R' can be any alkyl or aryl groups. ### Step 2: Analyze Carcinogenicity - **Aniline**: While aniline has been associated with some health risks, it is generally considered to be less carcinogenic compared to other compounds. It can be metabolized in the body to form potentially harmful substances, but its direct carcinogenic effects are relatively low. ...
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ICSE-ORGANIC COMPOUNDS CONTAINING NITROGEN-EXERCISE (PART-I OBJECTIVE QUESTIONS)
  1. Gabriel phthalimide synthesis is used for the preparation of........

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  2. CH3 NH2(aq) turns........litmus........

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  3. Out of aniline and N-nitrosoamine........is carcinogenic

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  4. Carbylamine test is given by........amines.

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  5. Basicity of methylamine is......than that of ammonia.

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  6. Methylamine is more....than ammonia due to.....effect.

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  7. According to IUPAC system, CH3 CH2 CN is named as ...... while CH3 CH2...

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  8. All isocyanides on hydrolysis with water in presence of HCI yield.....

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  9. Alkyl cyanides are .... soluble in water than alkyl isocyanides.

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  10. Alkyl isocyanides can be converted into cyanides by .....

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  11. Alkyl cyanides generally have .... boiling points than isocyanides.

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  12. Diphenylamine is less ........ than aniline.

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  13. Reaction of aniline with ......... yields C6 H5 N underset(to )= C a...

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  14. Benzenediazonium chloride is formed when ........ is treated with .......

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  15. Butane nitrile can be prepared by heating

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  16. Phenyl isocyanides are prepared by

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  17. The compound obtained by reducing CH3 CN with Na//C2 H5 OH is

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  18. An isonitrile on reduction gives

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  19. Hydrolysis of benzonitrile gives

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  20. Conversion of nitrobenzene to aniline is carried out in

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