Arrange the following in the decreasing order of stability:
$I. CH_2=CH-CHO$
$II. ^+CH_2-CH=CH-O^-$
$III. ^-CH_2-CH=CH-O^+$

  • A
    $I > II > III$
  • B
    $III > II > I$
  • C
    $II > I > III$
  • D
    $I > III > II$

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Similar Questions

Correct statements for the given reaction are :
$A$. Compound '$B$' is aromatic
$B$. The completion of above reaction is very slow
$C$. '$A$' shows tautomerism
$D$. The bond lengths $C-C$ in compound $B$ are found to be same
Choose the correct answer from the options given below :

The correct order of decreasing length of the bond as indicated by the arrow in the following structures is:

The correct order of stability for the given canonical structures is:
$(I)$ $H-C(=O)-CH_2^-$
$(II)$ $H-C(O^-)(^+)-CH_2^-$
$(III)$ $H-C(O^-)=CH_2$

The correct stability order of the given canonical structures is:

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Which of the following is the most unstable resonance structure of the $p$-nitrophenoxide ion?

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