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(a)
Interpretation:
Whether the following molecule has a liquid crystalline phase or not should be determined.
Concept introduction:
Liquid crystals are defined as a phase in which substance exhibits properties of both liquids and solids. Liquid crystal flow like a liquid but their arrangement of the molecule as well as intermolecular forces is like solid.
Liquid crystal molecules are made up of six-membered rings with on terminal polar group, a linkage group and a side chain of carbon atoms. Each carbon atom in liquid crystal molecules has trigonal planar geometry.
The molecules are rigid. The rigidity is increased due to the presence of double-bonded linkage groups such as
The terminal polar groups exhibit strong intermolecular forces such as strong dipole-dipole interaction or dipole−induced dipole interaction and hydrogen bond.
Types of liquid crystal are as follows:
- Nematic Liquid crystal.
- Smectic Liquid crystal.
1. Nematic Liquid crystal: The molecules in the nematic phase are in the same direction and can move around freely very much like that of liquid. In this, the axis is parallel but the ends are not aligned.
2. Smectic Liquid crystal: The molecules in the smectic phase are perpendicular to the plane and are aligned in layers. In these, the long axis is parallel and also their ends are aligned.
(b)
Interpretation:
Whether the following molecule has a liquid crystalline phase or not should be determined.
Concept introduction:
Liquid crystals are defined as a phase in which substance exhibits properties of both liquids and solids. Liquid crystal flow like a liquid but their arrangement of the molecule as well as intermolecular forces is like solid.
Liquid crystal molecules are made up of six-membered rings with on terminal polar group, a linkage group and a side chain of carbon atoms. Each carbon atom in liquid crystal molecules has trigonal planar geometry.
The molecules are rigid. The rigidity is increased due to the presence of double-bonded linkage groups such as
The terminal polar groups exhibit strong intermolecular forces such as strong dipole-dipole interaction or dipole−induced dipole interaction and hydrogen bond.
Types of liquid crystal are as follows:
- Nematic Liquid crystal.
- Smectic Liquid crystal.
1. Nematic Liquid crystal: The molecules in the nematic phase are in the same direction and can move around freely very much like that of liquid. In this, the axis is parallel but the ends are not aligned.
2. Smectic Liquid crystal: The molecules in the smectic phase are perpendicular to the plane and are aligned in layers. In these, the long axis is parallel and also their ends are aligned.
(c)
Interpretation:
Whether the following molecule has a liquid crystalline phase or not should be determined.
Concept introduction:
Liquid crystals are defined as a phase in which substance exhibits properties of both liquids and solids. Liquid crystal flow like a liquid but their arrangement of the molecule as well as intermolecular forces is like solid.
Liquid crystal molecules are made up of six-membered rings with on terminal polar group, a linkage group and a side chain of carbon atoms. Each carbon atom in liquid crystal molecules has trigonal planar geometry.
The molecules are rigid. The rigidity is increased due to the presence of double-bonded linkage groups such as
The terminal polar groups exhibit strong intermolecular forces such as strong dipole-dipole interaction or dipole−induced dipole interaction and hydrogen bond.
Types of liquid crystal are as follows:
- Nematic Liquid crystal.
- Smectic Liquid crystal.
1. Nematic Liquid crystal: The molecules in the nematic phase are in the same direction and can move around freely very much like that of liquid. In this, the axis is parallel but the ends are not aligned.
2. Smectic Liquid crystal: The molecules in the smectic phase are perpendicular to the plane and are aligned in layers. In these, the long axis is parallel and also their ends are aligned.
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Chapter 11 Solutions
CHEMISTRY-W/MASTERING CHEMISTRY ACCESS
- Identify the missing organic reactants in the following reaction: X + Y H+ two steps Note: This chemical equation only focuses on the important organic molecules in the reaction. Additional inorganic or small-molecule reactants or products (like H2O) are not shown. In the drawing area below, draw the skeletal ("line") structures of the missing organic reactants X and Y. You may draw the structures in any arrangement that you like, so long as they aren't touching. Click and drag to start drawing a structure. Х :arrow_forwardDraw the mechanism of friedel-crafts acylation using acetyl chloride of m-Xylenearrow_forwardI need help naming these in IUPACarrow_forward
- H R Part: 1/2 :CI: is a/an electrophile Part 2 of 2 Draw the skeletal structure of the product(s) for the Lewis acid-base reaction. Include lone pairs and formal charges (if applicable) on the structures. 4-7: H ö- H Skip Part Check X :C1: $ % L Fi Click and drag to start drawing a structure. MacBook Pro & ㅁ x G 0: P Add or increase positive formal cha Save For Later Submit ©2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Centearrow_forwardDraw the friedel-crafts acylation mechanism of m-Xylenearrow_forwardDon't used hand raiting and don't used Ai solutionarrow_forward
- 1. Base on this experimental results, how do you know that the product which you are turning in is methyl 3-nitrobenzoate(meta substituted product ) rather than either of the other two products? 2. What observation suggests that at least a small amount of one or both of the other two isomers are in the mother liquor?arrow_forwardExplain Huckel's rule.arrow_forwardhere is my question can u help me please!arrow_forward
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