- Aphenol
- Bp-cresol
- Cm-nitrophenol
- Dp-nitrophenol
Explanation:
o-nitro phenol participates in intra-molecular H−bonding, which makes it less acidic than p-nitro phenol. Since acidic strength depends on the stability of negative ion after removal of acidic H, −NO2 group in o and p position provides −M effect as the negative charge delocalizes.
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$Ag\left( s \right)\left| {AgBr\left( s \right)\,\left| {B{r^ - }\left( {0.01\,M} \right)} \right|\,\left| {{I^ - }\left( {0.02\,M} \right)} \right|\,AgI\left( s \right)} \right|Ag\left( s \right)$
the correct information is
[Given : $K_{sp}\,\left( {AgBr} \right) = 4 \times {10^{ - 13}}$ ,
$K_{sp}\,\left( {AgI} \right)$ $ = 8 \times {10^{ - 17}},\frac{{2.303\,RT}}{F} = 0.06\,V,\,\log \,2 = 0.3]$
Product is