Benzene is a special case of conjugation that leads to an especially stable bonding arrangement. The benzene ring consists of six sp2 hybridized carbon atoms in a regular hexagon. Each carbon forms two σ-bonds with adjacent carbons‚ and a third σ-bond with a hydrogen atom. The 2p orbital on each atom is available for π-bonding. Interaction between the p orbitals on the six carbon atoms forms a conjugated system of π-electrons. Molecules with this bonding arrangement are called aromatic molecules
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Benzene 1 Benzene Benzene Identifiers [1] CAS number 71-43-2 PubChem 241 ChemSpider 236 UNII J64922108F EC number 200-753-7 KEGG C01407 ChEBI CHEBI:16716 ChEMBL CHEMBL277500 RTECS number CY1400000 Jmol-3D images Image 1 [2] [3] [4] [5] [6] [7] [8] [9] Properties Molecular formula CH Molar mass 78.11 g mol−1 Appearance Colorless liquid Odor aromatic‚ gasoline-like
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Benzene Benzene‚ C(6)H(6)‚ is a clear‚ colorless‚ flammable liquid that is insoluble in water.Its boiling point is 80 degrees C (176 degrees F). In the past benzene was obtained from the distillation of coal in the absence of air. Today most benzene is made syntheticallyfrom petroleum products. The benzene is a closed ring of six atoms connected by bonds that resonatebetween single and double bonds; each carbon is also bound to a single atom. Benzene isinsoluble in water but mixes
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The global market for linear alkyl benzene (LAB) is expected to reach USD 9.27 billion by 2020‚ according to a new study by Grand View Research‚ Inc. Growing demand for household cleaning & industrial cleaning particularly in emerging market of Asia Pacific is expected to remain a key driving factor for the market. However‚ volatile raw material price is expected to remain a key challenge for market participants. Linear alkylbenzene sulphonate (LAS) emerged as the leading application segment for
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Electrophilic Aromatic Substitution: Bromination of Aromatic Compounds Introduction: The experiment focuses on finding out what kind of activating effects that four different substituents will have on an aromatic benzene ring. The substituents being tested are aniline‚ anisole‚ acetamide (acetanilide)‚ and phenol. All four of these groups are either para or ortho activating. Bromination is the reaction that will be carried out. The melting point ranges of the final products will be taken in order
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Compounds- possess a ring shaped structure Benzene (C6H6)- aka. naphtha - unsaturated cyclic compound - simplest aromatic HC - all C to C bonds are identical; each C has a H atom - substitution reactions occur instead of addition reaction - delocalized pi bonding in benzene imparts stability (aromaticity); responsible for resistance to addition reactions (involve breaking delocalized bonding) Benzene Derivatives- produced when one or more H atoms on benzene is/ are replaced by new group/s such as alkyl
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March 13‚ 2015 Answers to Questions: 1.) Arrangement of Reactivity: (fastest to slowest) - Phenol‚ Nitrophenol‚ Acetanilide‚ Benzene‚ Chlorobenzene‚ Aniline - A reaction has occurred if there’s a change in color. The nature of the substituent‚ whether electron-donating to the ring or electron-withdrawing from the ring‚ was responsible for the reactivity of the benzene. Aniline and acetanilide contain amine groups‚ which are electron-donating. Chlorobenzene contains chlorine‚ which is electron-withdrawing
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of electrophilic aromatic substitution. A strongly charged electrophile‚ in this case a nitro group‚ replaces a proton on the aromatic ring. Aromatic compounds undergo substitution instead of addition to maintain resonance. The substituent on the benzene ring determines where the electrophile will add. Electron withdrawing substituents‚ like nitro group‚ withdraw electrons due to induction and direct position of the carbocation through resonance to add electrophile to meta position. Nitric acid‚ sulfuric
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Unsaturated Hydrocarbons Unsaturated hydrocarbons Have fewer hydrogen atoms attached to the carbon chain than alkanes. Are alkenes with double bonds. Are alkynes with triple bonds. 1 Structure of Alkenes Alkenes (and alkynes) are unsaturated hydrocarbons Alkenes have one or more double bonds The two bonds in a double bond are different: - one bond is a sigma () bond; these are cylindrical in shape and are very strong - the other is a pi (π) bond; these involve sideways overlap of
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industrially important intermediates. These compounds are prepared under efficient green protocol with high yield and shorter reaction time in presence of eco-friendly catalyst ZnO/ZrO2. These are prepared using unfunctionalized simple/substituted benzenes which are cheap‚ more abundant and renewable
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