For a reaction, `aA+bBhArrcC+dD`, the reaction quotient `Q=([C]_(0)^(c)[D]_(0)^(d))/([A]_(0)^(a)[B]_(0)^(b))`, where `[A]_(0)`, `[B]_(0)`, `[C]_(0)`, `[D]_(0)` are initial concentrations. Also `K_(c)=([C]^(c)[D]^(d))/([A]^(a)[B]^(b))` where `[A]`, `[B]`, `[C]`, `[D]` are equilibrium concentrations. The reaction proceeds in forward direction if `Q lt K_(c)` and in backward direction if `Q gt K_(c)`. The variation of `K_(c)` with temperature is given by: `2303log(K_(C_(2)))/(K_(C_(1)))=(DeltaH)/(R)[(T_(2)-T_(1))/(T_(1)T_(2))]`. For gaseous phase reactions `K_(p)=K_(c)(RT)^(Deltan)` where `Deltan=` moles of gaseous products `-` moles of gaseous reactants. Also `-DeltaG^(@)=2.303RT log_(10)K_(c)`. The equilibrium constant `K_(c)` for `A_((g))hArrB_((g))` is `1.1`. The gas having concentration `ge 1` is:A. `[B]` if `[A]=0.91`B. `[B]` if `0.9lt[A]le1`C. both `[A]` and `[B]` if `[A]gt1`D. all are correct