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The smectic liquid crystalline phase can be said to be more highly ordered than the nematic phase. In what sense is this true?

Short Answer

Expert verified
The smectic phase is more highly ordered than the nematic phase due to its additional positional order, with molecules arranged in layers.

Step by step solution

01

Understand Liquid Crystals

Liquid crystals are states of matter that have properties between those of conventional liquids and solid crystals. They are typically known for their fluidity similar to liquid but with some degree of ordering as in solids.
02

Define Nematic Phase

In the nematic phase, the molecules are oriented in the same direction, meaning they have long-range orientational order. However, the positions of the molecules are random, leading to no positional order.
03

Define Smectic Phase

The smectic phase also maintains orientational order like the nematic phase. However, unlike the nematic phase, the smectic phase has an additional layer of positional order, where molecules are organized in layers that can slide over each other.
04

Compare Ordering

The smectic phase is more ordered than the nematic phase because it has both orientational and some degree of positional order due to the layers. In contrast, the nematic phase only has orientational order without any positional order.
05

Conclusion

The smectic phase's higher order arises from its molecular arrangement in layers, providing it with both orientational and positional order, making it more ordered than the nematic phase, which lacks the positional aspect.

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Smectic Phase
The smectic phase is a fascinating state within the realm of liquid crystals. It combines the fluidity of liquids with certain structural characteristics of solids. In this phase, molecules arrange themselves in well-defined layers, similar to the pages of a book. Each of these layers is free to slide over one another, providing the material with fluid-like properties.
What's intriguing about the smectic phase is the high degree of order it exhibits. Within each layer, the molecules maintain a consistent orientation—this is known as orientational order. The position of molecules across the layers is also somewhat organized, adding another level of structural order, termed positional order. This kind of order gives smectic crystals unique properties, useful in various applications, from digital displays to tunable lenses.
  • Exhibits both orientational and positional order
  • Formed in layered structures
  • Retains some fluidity despite its structure
Nematic Phase
The nematic phase is perhaps the simplest liquid crystalline phase. In this state, the molecules mostly align parallel to each other, which is known as orientational order. However, unlike the smectic phase, there's no particular arrangement or ordering in the position of the molecules—they are free to move around like in a liquid.
This absence of positional order means that while nematic phases have structural orientation, they lack the layered structure of smectic phases. This gives nematic liquid crystals unique characteristics such as the ability to flow and adapt easily while maintaining a uniform direction. This feature makes them ideal for use in liquid crystal displays (LCDs), where the alignment of molecules can control light passage.
  • Has orientational order
  • No positional order
  • Suitable for LCD technology
Orientational Order
Orientational order is a key concept when discussing liquid crystals, particularly in phases like nematic and smectic. It refers to how the molecules in the liquid crystal phase align themselves in the same spatial direction. Imagine a group of aligned compass needles all pointing towards the same north direction—this is a visualization of orientational order.
This order is pivotal because it allows liquid crystals to manipulate light, which is why they are so important in display technology. The orderly orientation affects how the material interacts with electric fields and light, enabling precise control over transparency and reflection.
  • Alignment direction of molecules
  • Present in nematic and smectic phases
  • Essential for light manipulation in electronics
Positional Order
Positional order describes the arrangement of molecules in a regular, repeating pattern. This type of order is primarily seen in the smectic liquid crystalline phase. While the smectic phase shares orientational order with the nematic phase, the key difference lies in the additional positional order.
In the smectic phase, molecules are organized into layers, much like stacked sheets, adding a degree of order not present in the nematic phase. This arrangement is crucial for certain technological applications because it affects the mechanical and optical properties of the material. Understanding positional order helps in designing materials with specific requirements, such as elasticity and optical clarity.
  • Refers to molecule positioning
  • Seen in smectic phases
  • Influences material properties

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Most popular questions from this chapter

True or false: (a) \(\mathrm{CBr}_{4}\) is more volatile than \(\mathrm{CCl}_{4}\). (b) \(\mathrm{CBr}_{4}\) has a higher boiling point than \(\mathrm{CCl}_{4}\). (c) \(\mathrm{CBr}_{4}\) has weaker intermolecular forces than \(\mathrm{CCl}_{4}\). (d) \(\mathrm{CBr}_{4}\) has a higher yapor pressure at the same temperature than \(C O\)

At \(25^{\circ} \mathrm{C}\) gallium is a solid with a density of \(5.91 \mathrm{~g} / \mathrm{cm}^{3} .\) Its melting point, \(29.8^{\circ} \mathrm{C}\), is low enough that you can melt it by holding it in your hand. The density of liquid gallium just above the melting point is \(6.1 \mathrm{~g} / \mathrm{cm}^{3}\). Based on this information, what unusual feature would you expect to find in the phase diagram of gallium?

Suppose the vapor pressure of a substance is measured at two different temperatures. (a) By using the Clausius-Clapeyron equation (Equation 11.1\()\) derive the following relationship between the vapor pressures, \(P_{1}\) and \(P_{2}\), and the absolute temperatures at which they were measured, \(T_{1}\) and \(T_{2}\) : $$ \ln \frac{P_{1}}{P_{2}}=-\frac{\Delta H_{\text {vap }}}{R}\left(\frac{1}{T_{1}}-\frac{1}{T_{2}}\right) $$ (b) Gasoline is a mixture of hydrocarbons, a component of which is octane \(\left(\mathrm{CH}_{3} \mathrm{CH}_{2} \mathrm{CH}_{2} \mathrm{CH}_{2} \mathrm{CH}_{2} \mathrm{CH}_{2} \mathrm{CH}_{2} \mathrm{CH}_{3}\right)\). Octane has a vapor pressure of \(1.86 \mathrm{kPa}\) at \(25^{\circ} \mathrm{C}\) and a vapor pressure of \(19.3 \mathrm{kPa}\) at \(75^{\circ} \mathrm{C}\). Use these data and the equation in part (a) to calculate the heat of vaporization of octane. \((\mathbf{c})\) By using the equation in part (a) and the data given in part (b), calculate the normal boiling point of octane. Compare your answer to the one you obtained from Exercise 11.81 . (d) Calculate the vapor pressure of octane at \(-30^{\circ} \mathrm{C}\).

Which type of intermolecular force accounts for each of these differences? (a) Acetone, \(\left(\mathrm{CH}_{3}\right)_{2} \mathrm{CO},\) boils at \(56^{\circ} \mathrm{C}_{i}\) dimethyl sulfoxide or \(\mathrm{DMSO},\left(\mathrm{CH}_{3}\right)_{2} \mathrm{SO},\) boils at \(189^{\circ} \mathrm{C} .(\mathbf{b})\) \(\mathrm{CCl}_{4}\) is a liquid at atmospheric pressure and room temperature, whereas \(\mathrm{CH}_{4}\) is a gas under the same conditions. \((\mathbf{c})\) \(\mathrm{H}_{2} \mathrm{O}\) boils at \(100{ }^{\circ} \mathrm{C}\) but \(\mathrm{H}_{2} \mathrm{~S}\) boils at \(-60{ }^{\circ} \mathrm{C}\). (d) 1 -propanol boils at \(97^{\circ} \mathrm{C}\), whereas 2 -propanol boils at \(82.6^{\circ} \mathrm{C}\). CC(C)=O DMSO

Indicate whether each statement is true or false: (a) The critical pressure of a substance is the pressure at which it turns into a solid at room temperature. (b) The critical temperature of a substance is the highest temperature at which the liquid phase can form. (c) Generally speaking, the higher the critical temperature of a substance, the lower its critical pressure. (d) In general, the more intermolecular forces there are in a substance, the higher its critical temperature and pressure.

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