Advertisements
Advertisements
प्रश्न
Classify the following compound as a primary, secondary and tertiary halide.
1-Bromobut-2-ene
विकल्प
Primary halide
Secondary halide
Tertiary halide
Advertisements
उत्तर
Primary halide
Explanation:
\[\ce{\underset{1-Bromobut-2-ene}{CH3HC = CHCH2Br}}\]
APPEARS IN
संबंधित प्रश्न
Draw the structure of major monohalo products in the following reaction:
Draw the structures of major monohalo products in each of the following reaction:
Name the following halide according to the IUPAC system and classify it as an alkyl, allyl, benzoyl (primary, secondary, tertiary), vinyl or aryl halide:
CH3CH2C(CH3)2CH2I
Name the following halide according to the IUPAC system and classify it as an alkyl, allyl, benzoyl (primary, secondary, tertiary), vinyl or aryl halide:
(CH3)3CCH2CH(Br)C6H5
Name the following halide according to the IUPAC system and classify it as an alkyl, allyl, benzoyl (primary, secondary, tertiary), vinyl or aryl halide:
CH3C(C2H5)2CH2Br
Name the following halide according to the IUPAC system and classify it as an alkyl, allyl, benzoyl (primary, secondary, tertiary), vinyl or aryl halide:
CH3C(Cl)(C2H5)CH2CH3
Draw the structure of major monohalo product in each of the following reactions :
m-Xylene reacts with Br2 in presence of FeBr3, what are products formed:
In which of the following molecules carbon atom marked with asterisk (*) is asymmetric?
(a) \[\begin{array}{cc}
\ce{H}\\
|\\
\phantom{.}\ce{C^*}\phantom{}\\
\phantom{}/\phantom{..}|\phantom{..}\backslash\phantom{}\\
\phantom{.}\ce{I}\phantom{...}\ce{Br}\phantom{..}\ce{Cl}
\end{array}\]
(b) \[\begin{array}{cc}
\ce{D}\\
|\\
\phantom{.}\ce{C^*}\phantom{}\\
\phantom{}/\phantom{..}|\phantom{..}\backslash\phantom{}\\
\phantom{.}\ce{I}\phantom{...}\ce{Br}\phantom{..}\ce{Cl}
\end{array}\]
(c) \[\begin{array}{cc}
\ce{H}\\
|\\
\phantom{.}\ce{C^*}\phantom{}\\
\phantom{}/\phantom{..}|\phantom{..}\backslash\phantom{}\\
\phantom{..}\ce{OH}\phantom{..}\ce{C2H5}\phantom{}\ce{CH3}
\end{array}\]
(d) \[\begin{array}{cc}
\ce{H}\\
|\\
\phantom{.}\ce{C^*}\phantom{}\\
\phantom{}/\phantom{..}|\phantom{..}\backslash\phantom{}\\
\phantom{..}\ce{H}\phantom{...}\ce{C2H5}\phantom{}\ce{CH3}
\end{array}\]
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 |
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:
Which of the following belongs to the class of vinyl halides?
Name the following halide according to the IUPAC system and classify it as alkyl, allyl, benzyl (primary, secondary, tertiary), vinyl, or aryl halide:
\[\ce{CH3C(C2H5)2CH2Br}\]
Name the following halide according to IUPAC system and classify them as alkyl, allyl, benzyl (primary, secondary, tertiary), vinyl or aryl halides:
\[\ce{CH3C(Cl)(C2H5)CH2CH3}\]
Name the following halide according to IUPAC system and classify them as alkyl, allyl, benzyl (primary, secondary, tertiary), vinyl or aryl halides:
\[\ce{CH3C(C2H5)2CH2Br}\]
Name the following halide 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 halide according to IUPAC system and classify as alkyl, allyl, benzyl (primary, secondary, tertiary), vinyl or aryl halide:
\[\ce{CH3C(C2H5)2CH2Br}\]
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 halides according to IUPAC system and classify them as alkyl, allyl, benzyl (primary, secondary, tertiary), vinyl or aryl halides:
\[\ce{CH3CH2C(CH3)2CH2I}\]
Write the structure of the following organic halogen compound.
4-tert-Butyl-3-iodoheptane
