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Match the following : {:("List - I",...

Match the following :
`{:("List - I","List - II"),((A) CH_(3)-CH(OH)-CHO,"(p) Carbohydrate"),((B) HOCH_(2)-CH(OH).CHO,"(q) Amino acid"),((C ) CH_(3)-CH(NH_(2)).COOH,"(r ) Positive Tollen's test"),((D) Ph.CH(CH_(2)NH_(2)).COOH,"(s) Ninhydrint test"):}`

Text Solution

Verified by Experts

The correct Answer is:
A-r; B-pr; C-qs; D-q
(A) `H-overset(CH_(3))overset("| ")underset("CHO")underset("| ")("C ")-OH rarr` Positive Tollen.s test
(B) `H-overset(CH_(2)OH)overset("| ")underset("CHO ")underset("| ")("C ")-OH rarr` It is a Carbohydrate, It gives positive Tollen.s test
(C ) `overset(CH_(3)" ")overset("| ")underset("COOH")underset("| ")("C ")H-NH_(2) rarr` It is an Amino acid, It gives Ninhydrint test.
(D)
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Match the following : {:(" List - I"," List - II"),((A) CH_(3)-underset(NH_(2))underset("|")("CH")-CH_(2)-overset(O)overset("||")("C")-OH,"(p) Exists as Zwitter ion in solid form"),((B) CH_(3)-CH_(2)-underset(NH_(2))underset("|")underset("CH")-COOH,"(q) On heating given diastereomeric product"),((C ) H_(2)N-CH_(2).CH_(2)CH_(2)-overset(O)overset("||")("C")OH,"(r ) On heating given a cyclic product"),((D) H_(2)N-CH_(2)-COOH,"(s) Treatment of ninhydrin gives blue colour"):}

{:("Column-I", "Column-II"), ( "A) "CH_(2)=CH-Cl, "P) +I effect"), ("B) "CH_(3)-CH=CH-O-CH_(3), "Q) -I effect"), ("C) "CH_(3)CH_(2)CH_(2)-Cl, "R) Hyperconjugation"), ("D) "CH_(3)-CH_(2)-CH_(2)-CH_(3), "S) Resonance"):}

Knowledge Check

  • CH_(3)CH_(2)NH_(2) is soluble in

    A
    Dilute HCI
    B
    `CuSo_(4)` solution
    C
    `AgNO_(3)`
    D
    dil. `H_(2)SO_(4)`

  • Match the following {:("List - I","List - II"),((A) CH_3COCH_3overset(Zn- Hg)underset(conc HCl)rarr,(1)CH_3CH_2OH),((B)CH_3CHOoverset(H_2.Ni)rarr,(2) CH_3CHO),((C)CH_3-CH=CH_2overset(H_2.Ni)rarr,(3) CH_3COCH_3),(,(4)CH_3CH_2CH_3),(,(5) CH_3CH_3):} The correct match is

    A
    `{:(A,B,C),(5,1,3):}`
    B
    `{:(A,B,C),(4,1,4):}`
    C
    `{:(A,B,C),(5,1,5):}`
    D
    `{:(A,B,C),(5,3,4):}`

  • Match the following {:(,"List I",,"List II"),(,,,"(Major"),(,,,"Product)"),((A),CH_(3)-CHBr-CH_(2)Broverset(KOH//C_(2)H_(5)OH)(rarr),(I),1^(@)-"alkyl bromide"),((B),CH_(3)-CH_(2)-CH = CH_(2)underset((C_(6)H_(5)CO)_(2)O_(2)", "Delta)overset(HBr)(rarr),(II),2^(@)-"alkyl bromide"),((C),CH_(3)CH_(2)CH_(3) overset(Br_(2), hv)(rarr),(III),"Allyl bromide"),((D),CH_(3)-CH=CH_(2) underset(Delta)overset(NBS)(rarr),(IV),"Alkenyl bromide"):} the correct answer is

    A
    `{:("A","B","C","D"),(I,IV,II,III):}`
    B
    `{:("A","B","C","D"),(IV,III,I,II):}`
    C
    `{:("A","B","C","D"),(II,III,I,IV):}`
    D
    `{:("A","B","C","D"),(IV,I,II,III):}`

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    CH_(3)CH_(2)CHO underset("reagent")overset("Tollens' ")rarr

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    The IUPAC name of the compound CH_(2)(OH)CH(NH_(2))COOH is

    The IUPAC name of the compound CH_2(OH)CH(NH_2)COOH is

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