Application organic chemistry

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17 Terms

1
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Functional group and disinfectant mechanism of rubbing alcohol

Contains a hydroxyl group (−OH-\text{OH}); acts as a disinfectant by disrupting microbial cell membranes and denaturing proteins.

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Structural feature and role of ethylene glycol in coolant mixtures

A diol containing two hydroxyl groups (−OH-\text{OH}); lowers water's freezing point and raises its boiling point to prevent freezing and overheating.

3
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Chemical basis and structural properties of polyethylene in plastic bottles

Synthesized from alkenes such as ethene; long covalently bonded polymer chains yield strong, durable, lightweight, and easily mouldable material.

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Functional group and solvent properties of acetone in nail polish remover

Acetone is a small molecule that can interfere w nail polish particles, it is a versatile solvent that dissolves nail polish because its polar carbonyl group and nonpolar carbon groups allow it to interact with different substances.

A ketone containing a carbonyl group (C=O\text{C=O}); functions as a polar solvent that dissolves polish resins and evaporates quickly due to high volatility.

5
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Functional group and sensory characteristics of ethyl ethanoate

An ester (−COO−-\text{COO}-); exhibits a pleasant, fruity scent and high volatility, making it suitable for perfumes and artificial flavourings.

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Evaporation rate comparison: water vs. acetone

Water evaporates more slowly because strong hydrogen bonding requires significant energy to separate molecules, whereas acetone relies on weaker dipole–dipole and dispersion forces.

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Evaporation rate comparison: ethanol vs. hexane

Ethanol evaporates more slowly because its combined hydrogen bonding, dipole–dipole, and dispersion forces are stronger than the London dispersion forces of hexane alone.

8
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Intermolecular mechanism causing water to form beads on wax

Strong cohesive hydrogen bonds among water molecules exceed the weak adhesive attractions to nonpolar wax, causing droplets to bead.

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Intermolecular mechanism causing water to bead on Teflon cookware

Teflon is nonpolar and forms very weak attractions with polar water; strong water–water hydrogen bonds keep water cohesive rather than spreading.

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Physical mechanism enabling propane gas to be stored as a liquid

Propane molecules have weak London dispersion forces; applied pressure forces molecules close enough together to condense the gas into a liquid at room temperature.

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Boiling point comparison: butane vs. octane

Octane has a higher boiling point because its larger molecular size contains more electrons, resulting in stronger London dispersion forces that require more thermal energy to overcome.

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Dual chemical properties that make ethanol an effective perfume solvent

Contains a polar −OH-\text{OH} group to hydrogen-bond alongside a nonpolar hydrocarbon region to dissolve aromatic compounds, while its volatility helps release scents.

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Structural basis for the moisturizing effect of glycerol

Contains three hydroxyl groups (−OH-\text{OH}) that form extensive hydrogen bonds with water molecules, attracting and retaining moisture in the skin.

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Solubility principle explaining why hexane dissolves nonpolar grease

'Like dissolves like': nonpolar hexane forms compatible dispersion attractions with nonpolar grease, whereas polar water cannot establish favorable attractions with grease.

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Why ethylene glycol is preferred over ethanol as an engine coolant

Features two −OH-\text{OH} groups that engage in strong hydrogen bonding with water, effectively depressing the freezing point and raising the boiling point while remaining less volatile.

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Boiling point comparison: methane vs. methanol

Methanol has a significantly higher boiling point because its −OH-\text{OH} group allows hydrogen bonding and dipole–dipole attractions, whereas nonpolar methane has only weak London dispersion forces.

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Chemical advantage of combining water and organic solvents in cleaning products

Polar water dissolves polar and ionic grime, while organic solvents dissolve nonpolar oils and grease, enabling the removal of a broader range of soils than water alone.