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International Conference on Organic Chemistry , will be organized around the theme “Innovation and advancement in organic chemistry”

Organic Chemistry 2016 is comprised of 15 tracks and 88 sessions designed to offer comprehensive sessions that address current issues in Organic Chemistry 2016.

Submit your abstract to any of the mentioned tracks. All related abstracts are accepted.

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Organic molecules contain carbon atoms. The carbon atoms are covalently bonded to other atoms, and various chains of carbon atoms can be found in most every molecule.carbon has four valence electrons, and therefore will make four bonds in accordance with the octet rule. All non-carbon-to-carbon bonds will be assumed to be carbon-hydrogen bonds, as hydrogen atoms are the most commonly found attached atom. Hydrogen has one valence electron, and will make one covalent bond. The carbon atom is capable of making single, double, and triple bonds, as well as bonding with oxygen, nitrogen, chlorine, or bromine. Oxygen has six valence electrons, and will make two covalent bonds. A single bond and a double bond are both possible for oxygen atoms. Nitrogen has five valence electrons, and will make three covalent bonds. Single, double, and triple bonds are all possibilities for nitrogen atoms. Chlorine and bromine each have seven valence electrons, and will make one covalent bond.

  • Track 1-1Nomenclature of new compounds
  • Track 1-2Types and characterization of organic compounds
  • Track 1-3Functional groups
  • Track 1-4Aliphatic compounds and aromatic compounds
  • Track 1-5Heterocyclic compounds

Organic molecules are described more commonly by drawings or structural formulas, combinations of drawings and chemical symbols.Lewis structures simplest model, additionally referred to as Lewis-dot diagrams, show the bonding relationship between atoms of a molecule and therefore the lone pairs of electrons within the molecule. Lewis structures also can be helpful in predicting molecular pure mathematics in conjunction with hybrid orbitals Resonance structures are used once one Lewis structure for ionic bonding one molecule cannot absolutely describe the bonding that takes place between close atoms relative to the empirical knowledge for the particular bond lengths between those atoms. Organic reactions are chemical reactions involving organic compounds. The basic organic chemistry reaction types are addition reactions, elimination reactions, substitution reactions, pericyclic reactions, rearrangement reaction, photochemical reactions and redox reactions. In organic synthesis, organic reactions are used in the construction of new organic molecules. The production of many man-made chemicals such as drugs, plastics, food additives, fabrics depend on organic reactions.Major reactions involved are free radical free-radical reaction is any chemical reaction involving free radicals. This reaction type is abundant in organic reactions. Rearrangement reaction is a broad class of organic reactions where the carbon skeleton of a molecule is rearranged to give a structural isomer of the original molecule.Often a substituent moves from one atom to another atom in the same molecule. In the example below the substituent R moves from carbon atom 1 to carbon atom 2.

  • Track 2-1Lewis structure: simplest model
  • Track 2-2Refined model: valence bond theory
  • Track 2-3Quantum mechanical model
  • Track 2-4Free radical and rearrangement reaction
  • Track 2-5Ionic reaction
  • Track 2-6Hydrolysis and condensation reaction

Organic reactions square measure chemical reactions involving organic compounds. The fundamental chemistry reaction sorts square measure addition reactions, elimination reactions, substitution reactions, pericyclic reactions, equilibrium reaction arranging reactions, chemistry reactions and oxidation-reduction reactions. Chemical reaction could be a reaction involving the breaking of a bond in an exceedingly molecule mistreatment water. The reaction primarily happens between associate particle and water molecules and sometimes changes the pH of an answer. In chemistry, there square measure 3 main styles of chemical reaction: salt hydrolysis, acid chemical reaction, and base chemical reaction. A condensation reaction, conjointly usually observed as dehydration synthesis, could be a reaction within which two molecules or moieties mix to make a bigger molecule, at the side of the loss of a little molecule. Once two separate molecules react, their condensation is termed unit.A straightforward example is that the condensation of two amino acids to make a amide.A radical is associate atom, molecule or particle that has unmated valency electrons. Associate atom or cluster of atoms that has a minimum of one unmated negatron and is so unstable and extremely reactive. In animal tissues, free radicals will harm cells and square measure believed to accelerate the progression of cancer science, upset, and age-related diseases

  • Track 3-1Thermodynamics
  • Track 3-2Enthalpy and entropy
  • Track 3-3Gibbs free energy
  • Track 3-4Redox reaction
  • Track 3-5First and second order reaction
  • Track 3-6Factors affecting rate of reaction

An understanding of chemical bond dipoles and also the varied kinds of noncovalent unit forces permits America to elucidate, on a molecular level, several evident physical properties of organic compounds. During this section, we are going to focus on solubility, freezing point, and boiling purpose. Boiling happens once the probability of warmth changing into internal energy and work to hold out vaporization becomes up to the probability of the reverse pathway. The boiling thermal property is higher the stronger the unit attractions as a result of the stronger the static force of attraction, the lot of energy is needed to separate the particles, the bigger the static P.E. increase related to vaporization. Ion-Ion forces or attractions area unit the strongest. They involve the attraction between species bearing at least a full charge and a species bearing a minimum of a full charge. The species concerned may be easy ions or advanced ions within the latter case, the charge is command by a covalent to certain species. For instance, the atoms among area unit covalently certain, however the general structure possesses a internet charge. Absolutely charged species area unit therefore drawn to one another that they will get terribly shut and kind intensive particle networks.Dipole-dipole force area unit significantly weaker than ion-ion forces, however if important for biological effect of chemicals, will have an oversized influence on physical properties. Dipole-dipole forces area unit necessary for molecules having internet dipole moments, molecules having atoms with differing electro negativities organized in such the simplest way that the middle of charge is totally different from the centre of charge.

  • Track 4-1U V spectroscopy
  • Track 4-2I R spectroscopy
  • Track 4-3NMR spectroscopy
  • Track 4-4Mass spectroscopy
  • Track 4-5Elemental analysis
  • Track 4-6Chromatography, Crystallography

Chemical reactions occur once collisions occur between atoms or molecules and there's ensuing modification within the arrangement of the chemical bonds. Therefore, rate of a reaction is proportional to the amount of collisions between molecules.  Not each collision can lead to a chemical reaction of the entire variety of collisions, solely a particular share can occur at the suitable energy to permit the processes of attractive force breaking and forming to occur. A first-order reaction may be a reaction that yield at a rate that depends linearly on just one chemical analysis. Differential rate laws area unit usually accustomed describe what's occurring on a molecular level throughout a reaction, whereas integrated rate laws area unit used for crucial the reaction order and also the worth of the speed constant from experimental measurements and chemical biology. Several necessary biological chemistry,like the formation of double-stranded deoxyribonucleic acid from two complementary strands, are often delineated mistreatment second order mechanics. During a second-order reaction, the total of the exponents within the rate law is capable .The speed of a second-order reaction could also be proportional to one concentration square  or to the merchandise of two concentrations the speed crucial step is that the slowest step of a chemical process that determines the speed at that the reaction yield.

  • Track 5-1Enzyme Kinetics, thermodynamic of enzymatic reactions
  • Track 5-2Polymer structure and morphology, properties of polymers
  • Track 5-3Polymer synthesis, polymer coating
  • Track 5-4Carbohydrates in life and medicine
  • Track 5-5Modern approaches in medicinal chemistry

Structure determination may be a procedure by that the three-dimensional atomic coordinates of a molecule or biomolecule square measure resolved victimisation associate analytical technique. several techniques square measure employed in structure determination, most typically X-ray physical science, proton magnetic resonance spectrographic analysis, microscopy and molecular modelling. Nuclear resonance is an analytical chemistry technique employed in internal control and research for determinative the content and purity of a sample additionally as its molecular structure.NMR may be wont to verify molecular conformation in answer additionally as finding out physical properties at the molecular level like conformational  ion exchange, part changes, solubility, and diffusion. Elemental analysis may be a method wherever a sample of some material is analyzed for its elemental and typically atom composition. Mass  is an analytical chemistry technique that helps determine the number and kind of chemistry gift during a sample by measure the mass-to-charge magnitude relation and abundance of gas-phase ions. A prism spectroscopy determines the mass of a molecule by measure the mass-to-charge magnitude relation of its particle diffusion. Ions square measure generated by causation either the loss or gain of a charge from a neutral species.

  • Track 6-1Organometallics compounds, structure, and bonding
  • Track 6-2Organometallic reactivity, organic synthesis
  • Track 6-3Early metal and f-block chemistry
  • Track 6-4Organic transformations in organometallics
  • Track 6-5Catalysis and commodities
  • Track 6-6Organometallic applications

Resonance or mesomerism may be a approach of describing delocalized electrons at intervals sure molecules or substance ions wherever the bonding can't be expressed by one single Lewis formula. Lewis structures, additionally referred to as Lewis-dot diagrams, show the bonding relationship between atoms of a molecule and therefore the lone pairs of electrons within the molecule. Lewis structures also can be helpful in predicting molecular pure mathematics in conjunction with hybrid orbitals Resonance structures are used once one Lewis structure for ionic bonding one molecule cannot absolutely describe the bonding that takes place between close atoms relative to the empirical knowledge for the particular bond lengths between those atoms. Internet total of valid resonance structures is outlined as a resonance hybrid, that represents the delocalization of electrons at intervals the molecule. A molecule that has many resonance structures is a lot of stable than one with fewer in organic macromolecular chemistry . Valence bond theory assumes every one bonds are localized bonds fashioned between two atoms by the donation of AN lepton from each atom. This is often truly AN invalid assumption as a result of several atoms bond victimisation delocalized electrons.

  • Track 7-1Biogeochemistry, soil biogeochemistry & marine biogeochemistry
  • Track 7-2Environmental biogeochemistry, ocean biogeochemistry
  • Track 7-3Petroleum geochemistry
  • Track 7-4Gas geochemistry
  • Track 7-5Organic hydrogeochemistry
  • Track 7-6Integrated perspectives in organic geochemistry
  • Track 7-7Biogeochemical cycles and inventors of biochemical elements
  • Track 7-8Thermogenic hydrocarbons in the contemporary environment
  • Track 7-9Analytical advances in organic geochemistry and implications
  • Track 7-10Transformation translocations and of organic chemicals

Energy exists in several forms, like heat, light, energy, and voltage. Energy is that the ability to bring forth modification or to try and do work. Physics is that the study of energy. First Law of Thermodynamics: Energy will be modified from one kind to a different; however it can't be created or destroyed. The whole quantity of energy and matter within the Universe remains constant, simply ever-changing from one kind to a different. The primary Law of physical model states that energy is usually preserved, it can't be created or destroyed. In essence, energy will be regenerate from one kind into another. The Second Law of physics states that "in all energy exchanges, if no energy enters or leaves the system, the P.E. of the state can forever be but that of the initial state this can be conjointly ordinarily observed as entropy. Within the method of energy transfer, some energy can dissipate as heat transfer. Entropy may be a live of disorder cells aren't disordered so have low entropy. The flow of energy maintains order and life. Entropy wins once organisms stop to require in internal energy and die. H is that the quantity of warmth content used or free in an exceedingly system at constant pressure. H is typically expressed because the modification in heat.

  • Track 8-1Modern experimental organic chemistry
  • Track 8-2Modern analytical organic chemistry
  • Track 8-3Modern theoretical organic chemistry
  • Track 8-4Modern organic synthesis
  • Track 8-5Nanocatalysts for organic synthetic transformations
  • Track 8-6Modern heterocyclic organic chemistry

Physical organic chemistry is the study of the relationship between structure and reactivity of organic molecules. More specifically, Modern physical organic chemistry applies the experimental tools of physical chemistry to the study of the structure of organic molecules and provides a theoretical framework that interprets how structure influences both mechanisms and rates of organic reactions. It can be thought of as a subfield that bridges organic chemistry with physical chemistry. Physical organic chemists use both experimental and theoretical disciplines such as spectroscopy, spectrometry, crystallography, and computational chemistry, and quantum theory to study both the rates of organic reactions and the relative chemical stability of the starting materials, transition states, and products. Chemists in this field work to understand the physical underpinnings of organic chemistry, and therefore physical organic chemistry applications in specialized areas including polymer chemistry, supramolecular chemistry, electrochemistry, and photochemistry

  • Track 9-1Biophysical Chemistry
  • Track 9-2Chemical structure and chemical Kinetics
  • Track 9-3Thermochemistry, quantum chemistry
  • Track 9-4Pharmaceutical Physical Chemistry

The rapid evolution in organic synthesis in recent years has seen dramatic changes in chemical sciences. One need only mention a few terms to understand that chemical systems that did not exist twenty years ago have become as much a part of the repertoire of the synthetic organic chemist such as the use of advanced microwave technology, photocatalytic synthesis, flow chemistry, used of advanced nanomaterials in organic synthesis and new innovative greener technology (catalysts-free processes) to design corresponding entity in a benign way. Last few years, there are various green solvents introduced in several organic methodologies such as polyethylene glycol (PEG), glycerol, ionic liquid, supercritical carbon dioxide (scCO2 ) and water etc. It is well-known that water is the most benign solvent used for the organic synthesis and is a prime choice for organic chemists. The chemistry of water is relatively old tremendous organic methodology that was investigated in last 20 years. The aim of this editorial is to provide a brief overview of the most promising, alternative reaction methodologies that can be employed in organic synthesis with the drive of safer, more sustainable as well as low environmental impact processes, which are crucial to application of improved efficiencies for organic synthesis in industry. This editorial highlights the some selective catalyst-free reactions in aqueous media (in-water and onwater).

  • Track 10-1Green chemistry
  • Track 10-2Flow chemistry
  • Track 10-3Combinatorial Chemistry
  • Track 10-4Material chemistry
  • Track 10-5Microwave chemistry and microwave spectroscopy

Organic synthesis is a special branch of chemical synthesis and is concerned with the construction of organic compounds via organic reactions. Organic molecules often contain a higher level of complexity than purely inorganic compounds, so that the synthesis of organic compounds has developed into one of the most important branches of organic chemistry. There are several main areas of research within the general area of organic synthesis: total synthesis, semi synthesis, and methodology, Organic synthesis is a special branch of chemical synthesis and is concerned with the construction of organic compounds via organic reactions. Organic molecules often contain a higher level of complexity than purely compounds in inorganic bio chemistry, so that the synthesis of organic compounds has developed into one of the most important branches of organic chemistry. There are several main areas of research within the general area of organic synthesis: total synthesis, semi synthesis, and methodology, Electro synthesis in chemistry is the synthesis of chemical compounds in an electrochemical cell. The main advantage of electro synthesis over an ordinary redox reaction is avoidance of the potential wasteful other half-reaction and the ability to precisely tune the required potential. Electro chemical synthesis is actively studied as a science and also has many industrial applications of microbes. Organic material chemistry is to provide an overview of the relationships between molecular or solid state structures and material properties. This is an interdisciplinary course which aims to provide an understanding of how molecular structure affects the properties of materials. The course consists of three sections (synthesis, analysis and properties). The use of design rules and advanced characterisation methods in the development of modern materials will be highlighted.

  • Track 11-1Enantioselective / chiral synthesis
  • Track 11-2Process development and structure, function and mechanism
  • Track 11-3New synthetic methods and advances in catalysis
  • Track 11-4Process development and non-precious metal catalysis
  • Track 11-5Organic electrosynthesis and organic materials chemistry

Within the field of organic chemistry, the definition of natural products is usually restricted to mean purified organic compounds isolated from natural sources that are produced by the pathways of primary or secondary metabolism. Within the field of medicinal chemistry, the definition is often further restricted to secondary metabolites. Secondary metabolites are not essential for survival, but nevertheless provide organisms that produce them an evolutionary advantage. Many secondary metabolites are cytotoxic and have been selected and optimized through evolution for use as "chemical warfare" agents against prey, predators, and competing organisms, natural product is a chemical compound or substance produced by a living organism—that is, found in nature. In the broadest sense, natural products include any substance produced by life. Natural products can also be prepared by chemical synthesis (both semi synthesis and total synthesis) and have played a central role in the development of the field of organic chemistry by providing challenging synthetic targets. The term natural product has also been extended for commercial purposes to refer to nutri cosmetics, dietary supplements, and foods produced from natural sources without added artificial ingredients. Heterocyclic compounds can be usefully classified based on their electronic structure. The saturated heterocycles behave like the acyclic derivatives. Thus, piperidine and tetrahydrofuran are conventional amines and ethers, with modified steric profiles. Therefore, the study of heterocyclic chemistry focuses especially on unsaturated derivatives, and the preponderance of work and applications involves unstrained 5- and 6-membered rings. Included are pyridine, thiophene, pyrrole, and furan. Another large class of heterocycles are fused to benzene rings, which for pyridine, thiophene, pyrrole, and furan are quinoline, benzothiophene, indole, and benzofuran, respectively. Fusion of two benzene rings gives rise to a third large family of compounds, respectively the acridine, dibenzothiophene, carbazole, and dibenzofuran. The unsaturated rings can be classified according to the participation of the heteroatom in the pi system.

  • Track 12-1New methods for the synthesis of heterocyclic compounds
  • Track 12-2Catalysis in heterocyclic chemistry
  • Track 12-3Synthesis of heterocyclic natural products
  • Track 12-4Route optimization of biologically active heterocyles
  • Track 12-5Insights into the biosynthesis of heterocyclic natural products
  • Track 12-6New strategies to construct heterocyclic compounds
  • Track 12-7Design and synthesis of biologically active heterocyclic compounds
  • Track 12-8Heterocyles as tools impacting the study of human disease
  • Track 12-9Perspectives on heterocyclic chemistry

A rearrangement reaction is a broad class of organic reactions where the carbon skeleton of a molecule is rearranged to give a structural isomer of the original molecule. Often a substituent moves from one atom to another atom in the same molecule. In the example below the substituent R moves from carbon atom 1 to carbon atom 2. A rearrangement is not well represented by simple and discrete electron transfers represented by curly arrows in organic chemistry texts. The actual mechanism of alkyl groups moving, as in Wagner-Meerwein rearrangement, probably involves transfer of the moving alkyl group fluidly along a bond, not ionic bond-breaking and forming. In pericyclic reactions, explanation by orbital interactions give a better picture than simple discrete electron transfers. It is, nevertheless, possible to draw the curved arrows for a sequence of discrete electron transfers that give the same result as a rearrangement reaction, although these are not necessarily realistic. In allylic rearrangement, the reaction is indeed ionic.

  • Track 13-1Methods and Applications of Claisen Rearrangement and Condensation
  • Track 13-2Methods and Applications of Wittig Rearrangement, Wurtz-Fittig Reaction
  • Track 13-3Methods and Applications of Cope Rearrangement, Kolbe-Schmitt Reaction
  • Track 13-4Methods and Applications of Suzuki Coupling reactions, Paal-Knorr Pyrrole Synthesis
  • Track 13-5Methods and Applications of Pinacol Rearrangement,and Meerwein-Ponndorf-Verley Reduction
  • Track 13-6Methods and Applications of Benzilic Acid Rearrangement
  • Track 13-7Methods and Applications of Hofmann Elimination reactions

Computational chemistry is a branch of chemistry that uses computer simulation to assist in solving chemical problems. It uses methods of theoretical chemistry, incorporated into efficient computer programs, to calculate the structures and properties of molecules and solids. Its necessity arises from the fact that apart from relatively recent results concerning the hydrogen molecular ion. The quantum many-body problem cannot be solved analytically, much less in closed form. While computational results normally complement the information obtained by chemical experiments, it can in some cases predict hitherto unobserved chemical phenomena. It is widely used in the design of new drugs and materials. Computational studies can be carried out to find a starting point for a laboratory synthesis, or to assist in understanding experimental data, such as the position and source of spectroscopic peaks.Computational studies can be used to predict the possibility of so far entirely unknown molecules or to explore reaction mechanisms that are not readily studied by experimental means.Thus, computational chemistry can assist the experimental chemist or it can challenge the experimental chemist to find entirely new chemical objects.Several major areas may be distinguished within computational chemistry

  • Track 14-1The fundamentals of computational chemistry in quantum mechanics
  • Track 14-2Computational chemistry and molecular simulations methods
  • Track 14-3Modeling biomolecule-membrane interactions
  • Track 14-4Computer aided drug design and industrial applications

The chemical protective clothing market is segmented on the basis of fiber type, user type, end-use industry, and region. The chemical protective clothing market is projected to register a CAGR of 5.8% between 2015 and 2020 and is expected to reach a market size of USD 1.2 Billion by 2020. Europe is the largest market for chemical protective clothing in the world and is projected to retain this position over the next five years. This is because of the stringent government legislations for the use of chemical protective clothing in certain industries. The high growth rate of the market is also attributable to the growing industrial sector in emerging economies such as China, India, Japan, and Brazil.

 

The agrochemicals market is considered to be one of the most important segments of agri-inputs, due to the expanding commercial cultivation of high value crops to meet the rising diversified food demand. Agrochemicals are consequently seen as those products, which improves the return on investment and also aid in meeting farmer’s as well as consumer demands, from the economical and health perspective with increasing per hectare production of quality agricultural products. The adoption of new technologies that increases crop production through the optimal use of scarce resources such as land, water, and fertilizers is gaining attention in the field of agriculture. The high growth potential in emerging markets and untapped regions, provides new growth opportunities for the market players. The growth of this market is driven by growing farmer’s attention towards superior quality agrochemicals, which should be balanced and nutritive.

  • Track 15-1Trends in Global Chemical Production and Consumption
  • Track 15-2Trends in Production and Consumption of Industrial Chemicals
  • Track 15-3Trends in Production and Consumption of Agricultural Chemicals
  • Track 15-4Trends in Production and Consumption of Metals and fibers