
To analyze the given options and determine which statement is incorrect regarding the structure depicted, we need to understand the chemistry of the functional groups and the molecular structure shown.
Conclusion: The incorrect statement is that the structure can be oxidized to a dicarboxylic acid with Br2 water. This method does not typically lead to full oxidation to a dicarboxylic acid.
The compound shown is a monosaccharide with an aldehyde group (-CHO) and multiple hydroxyl (-OH) groups. When treated with Br$_2$ water, it is not oxidized to a dicarboxylic acid but rather forms a monocarboxylic acid, making option (1) incorrect.
Statement (2) is correct: Despite having a –CHO group, certain sugars like glucose do not respond to Schiff’s test.
Statement (3) is correct: There are 4 chiral (asymmetric) carbon atoms present in the structure.
Statement (4) is correct: The compound can exist in equilibrium with two other cyclic forms, $\alpha$-D-glucose and $\beta$-D-glucose.
Write the structures of the main products of the following reactions:
Alkyl halides undergoing nucleophilic bimolecular substitution reaction involve:
The IUPAC name of the following compound is:

Which of the following is the correct IUPAC name of the given organic compound (X)?
The structure of compound $ X $ is as follows:
$ \text{H}_3\text{C} - \text{CH}_3 - \text{CH} = \text{CH} - \text{H} - \text{Br} $
A sub-atomic particle of mass \( 10^{-30} \) kg is moving with a velocity of \( 2.21 \times 10^6 \) m/s. Under the matter wave consideration, the particle will behave closely like (h = \( 6.63 \times 10^{-34} \) J.s)