The vector stencils library "Chemical drawings" contains 81 symbols of organic compounds and functional groups for chemical drawing.
Use it to draw structural formulas of organic molecules, schemes of chemical reactions and organic chemistry diagrams.
"Structural drawings.
Organic molecules are described more commonly by drawings or structural formulas, combinations of drawings and chemical symbols. The line-angle formula is simple and unambiguous. In this system, the endpoints and intersections of each line represent one carbon, and hydrogen atoms can either be notated explicitly or assumed to be present as implied by tetravalent carbon. The depiction of organic compounds with drawings is greatly simplified by the fact that carbon in almost all organic compounds has four bonds, nitrogen three, oxygen two, and hydrogen one. ...
Organic reactions.
Organic reactions are chemical reactions involving organic compounds. While pure hydrocarbons undergo certain limited classes of reactions, many more reactions which organic compounds undergo are largely determined by functional groups. The general theory of these reactions involves careful analysis of such properties as the electron affinity of key atoms, bond strengths and steric hindrance. These issues can determine the relative stability of short-lived reactive intermediates, which usually directly determine the path of the reaction.
The basic reaction types are: addition reactions, elimination reactions, substitution reactions, pericyclic reactions, rearrangement reactions and redox reactions. ...
Each reaction has a stepwise reaction mechanism that explains how it happens in sequence - although the detailed description of steps is not always clear from a list of reactants alone.
The stepwise course of any given reaction mechanism can be represented using arrow pushing techniques in which curved arrows are used to track the movement of electrons as starting materials transition through intermediates to final products." [Organic chemistry. Wikipedia]
The chemical symbols example "Design elements - Chemical drawings" was created using the ConceptDraw PRO software extended with the Chemistry solution from the Science and Education area of ConceptDraw Solution Park.
Use it to draw structural formulas of organic molecules, schemes of chemical reactions and organic chemistry diagrams.
"Structural drawings.
Organic molecules are described more commonly by drawings or structural formulas, combinations of drawings and chemical symbols. The line-angle formula is simple and unambiguous. In this system, the endpoints and intersections of each line represent one carbon, and hydrogen atoms can either be notated explicitly or assumed to be present as implied by tetravalent carbon. The depiction of organic compounds with drawings is greatly simplified by the fact that carbon in almost all organic compounds has four bonds, nitrogen three, oxygen two, and hydrogen one. ...
Organic reactions.
Organic reactions are chemical reactions involving organic compounds. While pure hydrocarbons undergo certain limited classes of reactions, many more reactions which organic compounds undergo are largely determined by functional groups. The general theory of these reactions involves careful analysis of such properties as the electron affinity of key atoms, bond strengths and steric hindrance. These issues can determine the relative stability of short-lived reactive intermediates, which usually directly determine the path of the reaction.
The basic reaction types are: addition reactions, elimination reactions, substitution reactions, pericyclic reactions, rearrangement reactions and redox reactions. ...
Each reaction has a stepwise reaction mechanism that explains how it happens in sequence - although the detailed description of steps is not always clear from a list of reactants alone.
The stepwise course of any given reaction mechanism can be represented using arrow pushing techniques in which curved arrows are used to track the movement of electrons as starting materials transition through intermediates to final products." [Organic chemistry. Wikipedia]
The chemical symbols example "Design elements - Chemical drawings" was created using the ConceptDraw PRO software extended with the Chemistry solution from the Science and Education area of ConceptDraw Solution Park.
Chemical symbols
Entity Relationship Diagram Symbols
ERD symbols used for professional ERD drawing are collected in libraries from the Entity-Relationship Diagram (ERD) solution for ConceptDraw DIAGRAM.
The vector stencils library "Conformations" contains 32 symbols of ring conformations, Newman and Fisher projections for chemical and biochemical drawing the molecular models and structural formulas of organic molecules and biochemical metabolites. It is useful in stereochemistry for drawing spatial structures of conformers of organic molecules, and schemes of stereospecific chemical reactions in organic synthesis.
"In chemistry, conformational isomerism is a form of stereoisomerism in which the isomers can be interconverted exclusively by rotations about formally single bonds (refer to figure on single bond rotation). Such isomers are generally referred to as conformational isomers or conformers and, specifically, as rotamers. Rotations about single bonds are restricted by a rotational energy barrier which must be overcome to interconvert one conformer to another. Conformational isomerism arises when the rotation about a single bond is relatively unhindered. That is, the energy barrier must be small enough for the interconversion to occur.
Conformational isomers are thus distinct from the other classes of stereoisomers (i. e. configurational isomers) where interconversion necessarily involves breaking and reforming of chemical bonds. For example, L- & D and R- & S- configurations of organic molecules have different handedness and optical activities, and can only be interconverted by breaking one or more bonds connected to the chiral atom and reforming a similar bond in a different direction or spatial orientation.
The study of the energetics between different rotamers is referred to as conformational analysis. It is useful for understanding the stability of different isomers, for example, by taking into account the spatial orientation and through-space interactions of substituents. In addition, conformational analysis can be used to predict and explain product(s) selectivity, mechanisms, and rates of reactions." [Conformational isomerism. Wikipedia]
The chemical symbols example "Design elements - Conformations" was created using the ConceptDraw PRO software extended with the Chemistry solution from the Science and Education area of ConceptDraw Solution Park.
"In chemistry, conformational isomerism is a form of stereoisomerism in which the isomers can be interconverted exclusively by rotations about formally single bonds (refer to figure on single bond rotation). Such isomers are generally referred to as conformational isomers or conformers and, specifically, as rotamers. Rotations about single bonds are restricted by a rotational energy barrier which must be overcome to interconvert one conformer to another. Conformational isomerism arises when the rotation about a single bond is relatively unhindered. That is, the energy barrier must be small enough for the interconversion to occur.
Conformational isomers are thus distinct from the other classes of stereoisomers (i. e. configurational isomers) where interconversion necessarily involves breaking and reforming of chemical bonds. For example, L- & D and R- & S- configurations of organic molecules have different handedness and optical activities, and can only be interconverted by breaking one or more bonds connected to the chiral atom and reforming a similar bond in a different direction or spatial orientation.
The study of the energetics between different rotamers is referred to as conformational analysis. It is useful for understanding the stability of different isomers, for example, by taking into account the spatial orientation and through-space interactions of substituents. In addition, conformational analysis can be used to predict and explain product(s) selectivity, mechanisms, and rates of reactions." [Conformational isomerism. Wikipedia]
The chemical symbols example "Design elements - Conformations" was created using the ConceptDraw PRO software extended with the Chemistry solution from the Science and Education area of ConceptDraw Solution Park.
Molecular conformations and projections
Swim Lane Flowchart Symbols
How To use House Electrical Plan Software
You can use many of built-in templates, electrical symbols and electical schemes examples of our House Electrical Diagram Software.
ConceptDraw is a fast way to draw: Electrical circuit diagrams, Schematics, Electrical Wiring, Circuit schematics, Digital circuits, Wiring in buildings, Electrical equipment, House electrical plans, Home cinema, Satellite television, Cable television, Closed-circuit television.
House Electrical Plan Software works across any platform, meaning you never have to worry about compatibility again. ConceptDraw DIAGRAM allows you to make electrical circuit diagrams on PC or macOS operating systems.
Settlement Process Flowchart. Flowchart Examples
Download easy flowchart software to create settlement process flowcharts show steps of monthly settlement with your business quickly and easily.
The vector stencils library "Cable TV" contains 64 symbols of cable TV network equipment.
Use these shapes for drawing CATV system design floor plans, network topology diagrams, wiring diagrams and cabling layout schemes in the ConceptDraw PRO diagramming and vector drawing software.
The vector stencils library "Cable TV" is included in the Electric and Telecom Plans solution from the Building Plans area of ConceptDraw Solution Park.
Use these shapes for drawing CATV system design floor plans, network topology diagrams, wiring diagrams and cabling layout schemes in the ConceptDraw PRO diagramming and vector drawing software.
The vector stencils library "Cable TV" is included in the Electric and Telecom Plans solution from the Building Plans area of ConceptDraw Solution Park.
Output Directional Tap 1
Output Directional Tap 2
Output Directional Tap 3
Output Directional Tap 4
Output Directional Tap 5
2-way Splitter
3-way Splitter
4-way Splitter
AC Power Block
Bond
Down Guy
Building Guy and Anchor
Rock Guy with Anchor
Down Guy with Anchor
Pole-to-Pole Guy
Sidewalk Down Guy with Anchor
Sidewalk Down Guy
Slack Span Messenger Wire
Tensioned Messenger Wire w/out cable
Tensioned Messenger Wire
Ground
Joint Usage (Power & Telephone Pole)
-cable-tv---vector-stencils-library.png--diagram-flowchart-example.png)
Joint Usgae Pole with Transformer
Strut
Tree Guy with Anchor
Push Brace (smaller pole in actual relative position)
-cable-tv---vector-stencils-library.png--diagram-flowchart-example.png)
Extension Arm
Built CATV Pole
Proposed CATV Pole
Directional Tap 1
Directional Tap 2
Manhole
Telephone Pole
Riser Pole
Vault Handheld
Fixed Equalizer
Fixed Flat Attenuators
Other Supporting Structures
Pedestal - Underground Routing
Power Pole
Direct Buried Underground Routing
Duct Line Underground Routing
Line Terminations
2-Way Optical Splice Location
3-Way Optical Splice Location
4-Way Optical Splice Location
> 4-Way Optical Splice Location
Optical Amplifier
Cable AC Power Combiner
Optical Fiber Cable
Optical Connector
Wavelength Demultiplexer
Wavelength Multiplexer
Optical Transmitter
Optical Transmitter
Optical Node
Optical Splitter
Headend (Signal Processing)
-cable-tv---vector-stencils-library.png--diagram-flowchart-example.png)
Node
Primary Hub
Secondary Hub
Coaxial Splice
Power Supply
Variable Equalizer
The vector stencils library "Welding" contains 38 welding joint symbols to identify fillets, contours, resistance seams, grooves, surfacing, and backing.
Use it to indicate welding operations on working drawings.
"Welding is a fabrication or sculptural process that joins materials, usually metals or thermoplastics, by causing coalescence. This is often done by melting the workpieces and adding a filler material to form a pool of molten material (the weld pool) that cools to become a strong joint, with pressure sometimes used in conjunction with heat, or by itself, to produce the weld. This is in contrast with soldering and brazing, which involve melting a lower-melting-point material between the workpieces to form a bond between them, without melting the workpieces.
Many different energy sources can be used for welding, including a gas flame, an electric arc, a laser, an electron beam, friction, and ultrasound.
Welds can be geometrically prepared in many different ways. The five basic types of weld joints are the butt joint, lap joint, corner joint, edge joint, and T-joint (a variant of this last is the cruciform joint). Other variations exist as well - for example, double-V preparation joints are characterized by the two pieces of material each tapering to a single center point at one-half their height. Single-U and double-U preparation joints are also fairly common - instead of having straight edges like the single-V and double-V preparation joints, they are curved, forming the shape of a U. Lap joints are also commonly more than two pieces thick - depending on the process used and the thickness of the material, many pieces can be welded together in a lap joint geometry." [Welding. Wikipedia]
The shapes example "Design elements - Welding" was created using the ConceptDraw PRO diagramming and vector drawing software extended with the Mechanical Engineering solution from the Engineering area of ConceptDraw Solution Park.
Use it to indicate welding operations on working drawings.
"Welding is a fabrication or sculptural process that joins materials, usually metals or thermoplastics, by causing coalescence. This is often done by melting the workpieces and adding a filler material to form a pool of molten material (the weld pool) that cools to become a strong joint, with pressure sometimes used in conjunction with heat, or by itself, to produce the weld. This is in contrast with soldering and brazing, which involve melting a lower-melting-point material between the workpieces to form a bond between them, without melting the workpieces.
Many different energy sources can be used for welding, including a gas flame, an electric arc, a laser, an electron beam, friction, and ultrasound.
Welds can be geometrically prepared in many different ways. The five basic types of weld joints are the butt joint, lap joint, corner joint, edge joint, and T-joint (a variant of this last is the cruciform joint). Other variations exist as well - for example, double-V preparation joints are characterized by the two pieces of material each tapering to a single center point at one-half their height. Single-U and double-U preparation joints are also fairly common - instead of having straight edges like the single-V and double-V preparation joints, they are curved, forming the shape of a U. Lap joints are also commonly more than two pieces thick - depending on the process used and the thickness of the material, many pieces can be welded together in a lap joint geometry." [Welding. Wikipedia]
The shapes example "Design elements - Welding" was created using the ConceptDraw PRO diagramming and vector drawing software extended with the Mechanical Engineering solution from the Engineering area of ConceptDraw Solution Park.
Welding joint symbols
The vector stencils library "Aromatics" contains 23 symbols of aromatic rings for chemical drawing of molecular structural formulas and reaction mechanism schemes in organic chemistry.
"In organic chemistry, aromaticity is a chemical property describing the way in which a conjugated ring of unsaturated bonds, lone pairs, or empty orbitals exhibits a stabilization stronger than would be expected by the stabilization of conjugation alone. ... Aromaticity can also be considered a manifestation of cyclic delocalization and of resonance. This is usually considered to be because electrons are free to cycle around circular arrangements of atoms that are alternately single- and double-bonded to one another. These bonds may be seen as a hybrid of a single bond and a double bond, each bond in the ring identical to every other. This commonly seen model of aromatic rings, namely the idea that benzene was formed from a six-membered carbon ring with alternating single and double bonds (cyclohexatriene), was developed by Kekulé (see History section below). The model for benzene consists of two resonance forms, which corresponds to the double and single bonds superimposing to give rise to six one-and-a-half bonds. Benzene is a more stable molecule than would be expected without accounting for charge delocalization. ... Types of aromatic compounds. The overwhelming majority of aromatic compounds are compounds of carbon, but they need not be hydrocarbons. 1. Neutral homocyclics. Benzene, as well as most other annulenes (cyclodecapentaene excepted) with the formula CnHn where n is an even number, such as cyclotetradecaheptaene. 2. Heterocyclics. In heterocyclic aromatics (heteroaromats), one or more of the atoms in the aromatic ring is of an element other than carbon. This can lessen the ring's aromaticity, and thus (as in the case of furan) increase its reactivity. Other examples include pyridine, pyrazine, imidazole, pyrazole, oxazole, thiophene, and their benzannulated analogs (benzimidazole, for example). 3. Polycyclics. Polycyclic aromatic hydrocarbons are molecules containing two or more simple aromatic rings fused together by sharing two neighboring carbon atoms (see also simple aromatic rings). Examples are naphthalene, anthracene, and phenanthrene. 4. Substituted aromatics. Many chemical compounds are aromatic rings with other functional groups attached. Examples include trinitrotoluene (TNT), acetylsalicylic acid (aspirin), paracetamol, and the nucleotides of DNA. 5. Atypical aromatic compounds. Aromaticity is found in ions as well: the cyclopropenyl cation (2e system), the cyclopentadienyl anion (6e system), the tropylium ion (6e), and the cyclooctatetraene dianion (10e). Aromatic properties have been attributed to non-benzenoid compounds such as tropone. Aromatic properties are tested to the limit in a class of compounds called cyclophanes. A special case of aromaticity is found in homoaromaticity where conjugation is interrupted by a single sp³ hybridized carbon atom. When carbon in benzene is replaced by other elements in borabenzene, silabenzene, germanabenzene, stannabenzene, phosphorine or pyrylium salts the aromaticity is still retained. Aromaticity also occurs in compounds that are not carbon-based at all. Inorganic 6-membered-ring compounds analogous to benzene have been synthesized. Hexasilabenzene (Si6H6) and borazine (B3N3H6) are structurally analogous to benzene, with the carbon atoms replaced by another element or elements. In borazine, the boron and nitrogen atoms alternate around the ring." [Aromaticity. Wikipedia]
The organic compound structural formulas example "Aromatics - Vector stencils library" was created using the ConceptDraw PRO software extended with the Chemistry solution from the Science and Education area of ConceptDraw Solution Park.
"In organic chemistry, aromaticity is a chemical property describing the way in which a conjugated ring of unsaturated bonds, lone pairs, or empty orbitals exhibits a stabilization stronger than would be expected by the stabilization of conjugation alone. ... Aromaticity can also be considered a manifestation of cyclic delocalization and of resonance. This is usually considered to be because electrons are free to cycle around circular arrangements of atoms that are alternately single- and double-bonded to one another. These bonds may be seen as a hybrid of a single bond and a double bond, each bond in the ring identical to every other. This commonly seen model of aromatic rings, namely the idea that benzene was formed from a six-membered carbon ring with alternating single and double bonds (cyclohexatriene), was developed by Kekulé (see History section below). The model for benzene consists of two resonance forms, which corresponds to the double and single bonds superimposing to give rise to six one-and-a-half bonds. Benzene is a more stable molecule than would be expected without accounting for charge delocalization. ... Types of aromatic compounds. The overwhelming majority of aromatic compounds are compounds of carbon, but they need not be hydrocarbons. 1. Neutral homocyclics. Benzene, as well as most other annulenes (cyclodecapentaene excepted) with the formula CnHn where n is an even number, such as cyclotetradecaheptaene. 2. Heterocyclics. In heterocyclic aromatics (heteroaromats), one or more of the atoms in the aromatic ring is of an element other than carbon. This can lessen the ring's aromaticity, and thus (as in the case of furan) increase its reactivity. Other examples include pyridine, pyrazine, imidazole, pyrazole, oxazole, thiophene, and their benzannulated analogs (benzimidazole, for example). 3. Polycyclics. Polycyclic aromatic hydrocarbons are molecules containing two or more simple aromatic rings fused together by sharing two neighboring carbon atoms (see also simple aromatic rings). Examples are naphthalene, anthracene, and phenanthrene. 4. Substituted aromatics. Many chemical compounds are aromatic rings with other functional groups attached. Examples include trinitrotoluene (TNT), acetylsalicylic acid (aspirin), paracetamol, and the nucleotides of DNA. 5. Atypical aromatic compounds. Aromaticity is found in ions as well: the cyclopropenyl cation (2e system), the cyclopentadienyl anion (6e system), the tropylium ion (6e), and the cyclooctatetraene dianion (10e). Aromatic properties have been attributed to non-benzenoid compounds such as tropone. Aromatic properties are tested to the limit in a class of compounds called cyclophanes. A special case of aromaticity is found in homoaromaticity where conjugation is interrupted by a single sp³ hybridized carbon atom. When carbon in benzene is replaced by other elements in borabenzene, silabenzene, germanabenzene, stannabenzene, phosphorine or pyrylium salts the aromaticity is still retained. Aromaticity also occurs in compounds that are not carbon-based at all. Inorganic 6-membered-ring compounds analogous to benzene have been synthesized. Hexasilabenzene (Si6H6) and borazine (B3N3H6) are structurally analogous to benzene, with the carbon atoms replaced by another element or elements. In borazine, the boron and nitrogen atoms alternate around the ring." [Aromaticity. Wikipedia]
The organic compound structural formulas example "Aromatics - Vector stencils library" was created using the ConceptDraw PRO software extended with the Chemistry solution from the Science and Education area of ConceptDraw Solution Park.
Biphenyl
Pyrene
Triphenylene
Phenanthrene
Anthracene
Acenaphthylene
Naphthalene
Indene
Indene
Indene
Indene
Cyclopentadiene
1,3-Cyclohexadiene
Cyclohexadiene
1,4-Cyclohexadiene
Cyclohexene
Cyclohexadiene 2
Cyclopentadiene 2
Cyclopentene
Cyclopentadiene 3
Cyclobutadiene
Cyclopropene
Phenalene
Chemistry Drawings
that can be then successfully used in the field of science and education, on various conferences, and so on.
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- Flowchart | Common Flowchart Symbols
