
Interpretation:
The type of intermolecular forces in the following compound 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-MASTERINGCHEMISTRY W/ETEXT
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- Consider the following nucleophilic substitution reaction. The compound listed above the arrow is the solvent for the reaction. If nothing is listed over the arrow, then the nucleophile is also the solvent for the reaction. Part: 0/2 Part 1 of 2 Br acetone + I What is the correct mechanism for the reaction? Select the single best answer. OSN 1 OSN 2 X Part: 1/2 Part 2 of 2 Draw the products for the reaction. Include both the major organic product and the inorganic product. If more than one stereoisomer is possible, draw only one stereoisomer. Include stereochemistry where relevant. Click and drag to start drawing a structure. Х 5 ☐arrow_forwardTriethyloxonium tetrafluoroborate reacts with ethanol (CH3CH2OH) to give diethyl ether (CH3CH2OCH2CH3). BF triethyloxonium tetrafluoroborate Which equation, including the curved arrows, best represents the rate-determining step in the mechanism? Select the single best answer. O OH CH3CH2 OH + H. 0+ CH₂H₂ :0 + 0+ ж + H + :0: 0 Carrow_forwardCH3CH2CH=CH2 + H₂O − H+arrow_forward
- Г C-RSA CHROMATOPAC CH=1 DATA 1: @CHRM1.C00 ATTEN=10 SPEED= 10.0 0.0 b.092 0.797 1.088 1.813 C-RSA CHROMATOPAC CH=1 Report No. =13 ** CALCULATION REPORT ** DATA=1: @CHRM1.000 11/03/05 08:09:52 CH PKNO TIME 1 2 0.797 3 1.088 4 1.813 AREA 1508566 4625442 2180060 HEIGHT 207739 701206 V 287554 V MK IDNO CONC NAME 18.1447 55.6339 26.2213 TOTAL 8314067 1196500 100 C-R8A CHROMATOPAC CH=1 DATA 1: @CHRM1.C00 ATTEN=10 SPEED= 10.0 0. 0 087 337. 0.841 1.150 C-R8A CHROMATOPAC CH=1 Report No. =14 DATA=1: @CHRM1.000 11/03/05 08:12:40 ** CALCULATION REPORT ** CH PKNO TIME AREA 1 3 0.841 1099933 41.15 4039778 HEIGHT MK IDNO 170372 649997¯¯¯ CONC NAME 21.4007 78.5993 TOTAL 5139711 820369 100 3 C-R8A CHROMATOPAC CH=1 DATA 1: @CHRM1.C00 ATTEN=10 SPEED= 10.0 0.100 0:652 5.856 3 1.165 C-RSA CHROMATOPAC CH-1 Report No. =15 DATA=1: @CHRM1.000 11/03/05 08:15:26 ** CALCULATION REPORT ** CH PKNO TIME AREA HEIGHT MK IDNO CONC NAME 1 3 3 0.856 4 1.165 TOTAL 1253386 4838738 175481 708024 V 20.5739 79.4261 6092124…arrow_forwardIndicate the product that is obtained if the benzotriazole reacts with the use of a medium basic product.arrow_forwardIndicate the product that is obtained if the benzotriazol reacts with dimethyl sulfate.arrow_forward
- Indicate how to obtain 2-metilbencimidazol from 1,2-diaminobenzene.arrow_forwardbreak down both reactions shown and explain it correctly using the bromonium ion mechanism, instead of the (disproven) carbocation-based mechanism.arrow_forwardIndicate how from 1,2-diaminobenzene to obtain 1-metilbenzotriazol.arrow_forward
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