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कर्नाटक बोर्ड पी.यू.सी.पीयूसी विज्ञान 2nd PUC Class 12

Name the following halide according to the IUPAC system and classify it as an alkyl, allyl, benzyl (primary, secondary, tertiary), vinyl or aryl halide: (CH3)3CCH2CH(Br)C6H5

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प्रश्न

Name the following halide according to the IUPAC system and classify it as an alkyl, allyl, benzyl (primary, secondary, tertiary), vinyl or aryl halide:

(CH3)3CCH2CH(Br)C6H5

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अति संक्षिप्त उत्तर
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उत्तर

IUPAC Name: 1-bromo-3,3-dimethyl-1-phenylbutane

Classification: Secondary (2°) benzyl halide

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अध्याय 6: Haloalkanes and Haloarenes - Exercises [पृष्ठ १८९]

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एनसीईआरटी Chemistry Part 1 and 2 [English] Class 12
अध्याय 6 Haloalkanes and Haloarenes
Exercises | Q 6.1 (iv) | पृष्ठ १८९
नूतन Chemistry [English] Class 12 ISC
अध्याय 6 Haloalkanes and Haloarenes
SHORT ANSWER TYPE QUESTIONS | Q 38. (d) | पृष्ठ ६१२

संबंधित प्रश्न

Draw the structure of the major monohalo product in the following reaction:


Name the following halide according to the IUPAC system and classify it as an alkyl, allyl, benzyl (primary, secondary, tertiary), vinyl or aryl halide:

o-Br-C6H4CH(CH3)CH2CH3


Identify the compound Y in the following reaction.


Which is the correct IUPAC name for \[\begin{array}{cc}
\ce{CH3 - CH - CH2 - Br}\\
\phantom{}|\phantom{.......}\\
\phantom{}\ce{C2H5}\phantom{....}
\end{array}\]?


Which of the following compounds can be classified as aryl halides?

(i) \[\ce{p-ClC6H4CH2CH(CH3)2}\]

(ii) \[\ce{p-CH3CHCl(C6H4)CH2CH3}\]

(iii) \[\ce{o-BrH2C - C6H4CH(CH3)CH2CH3}\]

(iv) \[\ce{C6H5 - Cl}\]


Match the structures of compounds given in Column I with the classes of compounds given in Column II.

  Column I Column II
(i) \[\begin{array}{cc}
\ce{CH3 - CH - CH3}\\
|\phantom{..}\\
\ce{X}\phantom{..}
\end{array}\]
(a) Aryl halide
(ii) \[\ce{CH2 = CH - CH2 - X}\] (b) Alkyl halide
(iii) (c) Vinyl halide
(iv) \[\ce{CH2 = CH - X}\] (d) Allyl halide

Classify the following compound as a primary, secondary and tertiary halide.

4-Bromopent-2-ene


Why are haloalkanes more reactive towards nucleophilic substitution reactions than haloarenes and vinylic halides?


Two isomers (A) and (B) with molar mass 184 g/mol and elemental composition C 52.2%; H 4.9% and Br 42.9% gave benzoic acid and p-bromobenzoic acid, respectively on oxidation with KMnO4. Isomer ‘A’ is optically active and gives a pale yellow precipitate when warmed with alcoholic AgNO3. Isomer ‘A’ and ‘B’ are, respectively:


Name the following halides according to IUPAC system and classify them as alkyl, allyl, benzyl (primary, secondary, tertiary), vinyl or aryl halides:

\[\ce{CH3C(C2H5)2CH2Br}\]


Name the following halides according to the IUPAC system and classify them as alkyl, allyl, benzyl (primary, secondary, tertiary), vinyl or aryl halides:

CH3C(C2H5 )2CH2Br


Name the following halide according to IUPAC system and classify it as alkyl, allyl, benzyl (primary, secondary, tertiary), vinyl or aryl halides:

\[\ce{CH3C(Cl)(C2H5)CH2CH3}\]


Name the following halides according to IUPAC system and classify them as alkyl, allyl, benzyl (primary, secondary, tertiary), vinyl or aryl halides:

\[\ce{CH3CH2C(CH3)2CH2I}\]


Name the following halides according to IUPAC system and classify them as alkyl, allyl, benzyl (primary, secondary, tertiary), vinyl or aryl halides:

\[\ce{CH3C(C2H5)2CH2Br}\]


Name the following halide according to IUPAC system and classify them as alkyl, allyl, benzyl (primary, secondary, tertiary), vinyl or aryl halide:

\[\ce{CH3C(CI)(C2H5)CH2CH3}\]


Name the following halide according to IUPAC system and classify as alkyl, allyl, benzyl (primary, secondary, tertiary), vinyl or aryl halides:

\[\ce{CH3C(C2H5)2CH2Br}\]


Draw the structure of the major monohalo product in the following reaction:


Name the following halide according to IUPAC system and classify them as alkyl, allyl, benzyl (primary, secondary, tertiary), vinyl or aryl halides:

\[\ce{CH3C(C2H5)2CH2Br}\]


IUPAC name of \[\begin{array}{cc}
\phantom{}\ce{CH3}\phantom{..........}\ce{Br}\phantom{........}\\
\phantom{}|\phantom{................}|\phantom{.........}\\
\phantom{}\ce{CH3CHCH2CHCHCH2CH3}\phantom{}\\
\phantom{}|\phantom{..}\\
\phantom{..}\ce{CH3}\phantom{}
\end{array}\] is ______.


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