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Test 3:Disubstituted Cycloalkanes definitions
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Chirality
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Chirality
Property where a molecule cannot be superimposed on its mirror image, often due to lack of symmetry or presence of stereocenters.
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Test 3:Disubstituted Cycloalkanes quiz
Test 3:Disubstituted Cycloalkanes
15 용어
Test 3: Disubstituted Cycloalkanes
5. Chirality
7 문제점
주제
Johnny
What is the Relationship Between Isomers?
5. Chirality
8 문제점
주제
Ernest
5. Chirality - Part 1 of 4
4 주제
15 문제점
장
Johnny
5. Chirality - Part 2 of 4
6 주제
15 문제점
장
Johnny
5. Chirality - Part 3 of 4
6 주제
15 문제점
장
Johnny
5. Chirality - Part 4 of 4
2 주제
5 문제점
장
00:35
Is the following disubstituted cyclobutane chiral?
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03:52
Three types of disubstituted cycloalkanes
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00:22
Is the following disubstituted cyclopropane chiral?
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이 집합의 용어 (15)
하이드의 정의
Chirality
Property where a molecule cannot be superimposed on its mirror image, often due to lack of symmetry or presence of stereocenters.
Disubstituted Cycloalkane
Cyclic compound featuring two identical groups attached at specific positions on the ring, influencing symmetry and chirality.
Geminal Disubstitution
Arrangement where two identical groups are bonded to the same carbon atom within a ring, always resulting in achirality.
Para Disubstitution
Configuration where two identical groups are attached to carbons directly across from each other on an even-membered ring.
Middle Disubstitution
Situation where two identical groups are attached at positions between geminal and para, with chirality depending on their orientation.
Cis Isomer
Form where two substituents are on the same side of a ring, often leading to meso compounds or achirality in cycloalkanes.
Trans Isomer
Form where two substituents are on opposite sides of a ring, typically resulting in chirality for disubstituted cycloalkanes.
Meso Compound
Molecule with multiple stereocenters and an internal plane of symmetry, rendering it achiral despite chiral centers.
Chair Conformation
Three-dimensional shape adopted by cyclohexane rings, minimizing strain and affecting the spatial arrangement of substituents.
Axial Position
Orientation in a chair conformation where a substituent points perpendicular to the average plane of the ring.
Equatorial Position
Orientation in a chair conformation where a substituent extends outward, roughly parallel to the ring plane, reducing steric hindrance.
Plane of Symmetry
Imaginary plane dividing a molecule into two mirror-image halves, indicating achirality if present.
Stereocenter
Atom, typically carbon, bonded to four different groups, giving rise to non-superimposable mirror images.
Equilibrium
Dynamic state where cyclohexane rapidly interconverts between chair forms, influencing overall molecular symmetry.
Even-Numbered Ring
Cyclic structure with an even count of atoms, allowing for para disubstitution and specific symmetry properties.