Question
Write the structure of the following compound.2-Hydroxycyclopentane carbaldehyde.

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Read the given passage and answer the questions number 1 to 5 that follow:
The substitution reaction of alkyl halide mainly occurs by $S_N1$ or $S_N2$ mechanism. Whatever mechanism alkyl halides follow for the substitution reaction to occur, the polarity of the carbon halogen bond is responsible for these substitution reactions. The rate of $S_N1$ reactions are governed by the stability of carbocation whereas for $S_N2$ reactions steric factor is the deciding factor. If the starting material is a chiral compound, we may end up with an inverted product or racemic mixture depending upon the type of mechanism followed by alkyl halide. Cleavage of ethers with HI is also governed by steric factor and stability of carbocation, which indicates that in organic chemistry, these two major factors help us in deciding the kind of product formed.
Predict the stereochemistry of the product formed if an optically active alkyl halide undergoes substitution reaction by $S_N2$ mechanism.
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Smoke passed through charged plates before allowing it to come out of chimneys in factories.
Name the alkene which will yield 1-chloro-1-methylcyclohexane by its reaction with HCl. Write the reactions involved.
Write IUPAC names of the following compound:$\text{CH}_3-\text{CH}_2-\text{O}-\text{CH}-\text{CH}_2-\text{CH}_3\\\ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ |\\\ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \ \text{CH}_3$
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A metal ion $M^{n+}$ having $d^4$ valence electronic configuration combines with three bidentate ligands to form a complex compound. Assuming $\triangle _ {0} > \text{P}$ :
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Draw the structure of the following compound.
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