- AMaltose
- ✓Sucrose
- CMannose
- DFructose
Sucrose is not a reducing sugar because it does not have an available hydroxyl group. The glycosidic bond that forms in sucrose occurs between the anomeric carbons on glucose and fructose which eliminates the availability of the hydroxyl group. The anomeric carbon is the carbon where the ring forms between the hydroxyl carbon and the carbonyl carbon.
Without this hydroxyl group, the ring cannot open and close and therefore not undergo mutarotation. Reducing sugars can undergo mutarotation. Nonreducing sugars cannot undergo mutarotation.
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| $Cl_2(g) \rightarrow 2Cl(g),$ | $242.3\,kJ\,mol^{-1}$ |
| $I_2(g) \rightarrow 2I(g),$ | $151.0\,kJ\,mol^{-1}$ |
| $ICl(g) \rightarrow I(g)+Cl(g),$ | $211.3\,kJ\,mol^{-1}$ |
| $I_2(s) \rightarrow I_2(g),$ | $62.76\,kJ\,mol^{-1}$ |
Given that the standard states for iodine and chlorine are $I_2(s)$ and $Cl_2(g),$ the standard enthalpy of formation for $ICl(g)$ is : ............... $\mathrm{kJ\,mol}^{-1}$
