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Classify the CH(3)-underset(CH(3))unders...

Classify the `CH_(3)-underset(CH_(3))underset(|)overset(CH_(3))overset(|)C-CH_(2)OH` as primary , secondary and tertiary alcohols.

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Primary alcohols
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Monomer of (-underset(CH_(3))underset(|)overset(CH_(3))overset(|)(C)-CH_(2)-)_(n) is

Classify the H_(2)C=CH-CH_(2)OH as primary , secondary and tertiary alcohols.

Monomer is [-CH_(2)-underset(COOCH_(3))underset(|)overset(CH_(2))overset(|)(C)-]_(n) is

Write the common & IUPAC name of CH_(3)-underset(CH_(3))underset(|)overset(CH_(3))overset(|)C-OH

Name the CH_(3)-underset(CH_(3))underset(|)C=underset(Br)underset(|)C-CH_(2)OH compound according to IUPAC system.

The following is not an appropriate reaction for the preparation of t-butyl ethyl ether. C_(2)H_(5)O"Na"+CH_(3)-underset(CH_(3))underset(|)overset(CH_(3))overset(|)C-Cl to CH_(3)-underset(CH_(3))underset(|)overset(CH_(3))overset(|)C-OC_(2)H_(5) What would be the major product of this reaction ?

The following is not an appropriae reaction for the preparation of t-butyl ethyl ether. C_(2)H_(5)ONa+CH_(3)-underset(CH_(3))underset(|)overset(CH_(3))overset(|)C-Cl to CH_(3)-underset(CH_(3))underset(|)overset(CH_(3))overset(|)C-OC_(2)H_(5) i) What would be the major product of this reaction ? ii) Write a suitable reaction for the preparation of t-butylethyl ether

Give the major products that are formed by heating of the CH_(3)-CH_(2)-CH_(2)-O-underset(CH_(3))underset(|)overset(CH_(3))overset(|)C-CH_(2)-CH_(3) ethers with HI.

The major product obtained in the following reaction is C_(2)H_(5)ONa + CH_(3)- underset(CH_(3))underset(|)overset(CH_(3))overset(|)(C) - Cl rarr

Knowledge Check

  • Monomer of (-underset(CH_(3))underset(|)overset(CH_(3))overset(|)(C)-CH_(2)-)_(n) is

    A
    2-methyl propene
    B
    Styrene
    C
    Propylene
    D
    Ethene
  • Monomer is [-CH_(2)-underset(COOCH_(3))underset(|)overset(CH_(2))overset(|)(C)-]_(n) is

    A
    Methyl methyl acrylate
    B
    Styrene
    C
    Propylene
    D
    Ethene
  • The major product obtained in the following reaction is C_(2)H_(5)ONa + CH_(3)- underset(CH_(3))underset(|)overset(CH_(3))overset(|)(C) - Cl rarr

    A
    `CH_(3) - underset(CH_(3))underset(|)overset(CH_(3))overset(|)(C) - O - C_(2)H_(5)`
    B
    `CH_(2) = underset(CH_(3))underset(|)(CH) - CH_(3)`
    C
    `CH_(3) = underset(CH_(3))underset(|)(CH) - O - C_(2)H_(5)`
    D
    `CH_(3)- underset(CH_(3))underset(|)overset(CH_(3))overset(|)(C) -CH_(2)CHO`
  • VIKRAM PUBLICATION ( ANDHRA PUBLICATION)-ORGANIC COMPOUNDS CONTAINING C,H AND O-INTEXT QUESTIONS
    1. Classify the CH(3)-underset(CH(3))underset(|)overset(CH(3))overset(|)C...

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    2. Classify the H(2)C=CH-CH(2)OH as primary , secondary and tertiary alc...

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    3. Classify the following as primary, secondary and tertiary alcohols: ...

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    4. Classify the as primary , secondary and tertiary alcohols.

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    5. Classify the following as primary, secondary and tertiary alcohols: ...

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    6. Classify the as primary , secondary and tertiary alcohols.

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    7. Identify the allylic alcohols in the above examples.

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    8. Name the CH(3)-CH(2)-underset(CH(2)Cl)underset(|)CH-overset(CH(2)OH)ov...

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    9. Name the CH(3)-underset(CH(3))underset(|)CH-CH(2)-underset(OH)underset...

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    10. Name the compound according to IUPAC system.

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    11. Name the H(2)C=CH-underset(OH)underset(|)CH-CH(2)-CH(2)-CH(3) compoun...

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    12. Name the CH(3)-underset(CH(3))underset(|)C=underset(Br)underset(|)C-CH...

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    13. Show how are the CH(3)-underset(CH(3))underset(|)CH-CH(2)OH alcohol p...

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    14. Show how are the alcohol prepared by the reaction of a suitable Grig...

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    15. Write structure of the products of the CH(3)-CH=CH(2) overset(H(2)O//H...

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    16. Write structure of the products of the

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    17. Write structure of the products of the CH(3)-CH(2)-underset(CH(3))und...

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    18. Predict the major product of acid catalysed dehydration of 1-methycycl...

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    19. Predict the major product of acid catalysed dehydration of butan-1-ol.

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    20. Write the reactions of Williamson synthesis of 2-ethoxy-3-methypentane...

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