"Bromination of alkenes stilbene tribromide" Essays and Research Papers

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    Reactions of hydrocarbons

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    molecules to join together. This is the reversed for a decrease in temperature the molecules move around less so there is less interaction between solute and solvent. We also differentiated alkanes and alkenes. Alkanes only contain c-c single bonds‚ are saturated‚ and are the least reactive. Alkenes are c=c double bonds‚ more reactive than alkanes‚ and unsaturated. In the next part of the experiment we added

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    Lab Protocol #8 - Dehydration of 3‚3-dimethyl-2-butanol KEYWORDS: alkenes‚ E2‚ E1‚ carbocation stability‚ elimination A. Introduction. The dehydration of alcohols is an ELIMINATION reaction that is commonly used to form alkene molecules. The mechanism for the dehydration of alcohols consists of transforming the –OH functional group into a better leaving group by using a strong acid to protonate the alcohol. After –OH has been transformed into –OH2+‚ it becomes easier to break the σ-bond between the

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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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    Cracking and Crude Oil

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    branched chains having different boiling points to straight chains Suggest how cracking can be used to obtain more useful alkanes and alkenes of lower Mr from larger hydrocarbon molecules The breaking up or large hydrocarbon chains into smaller molecules for alternative uses. Cracking produces a mixture containing mainly alkanes‚ alkenes or hydrogen. Alkenes are industrially useful molecules and smaller alkanes are used in fuels such as petrol. Thermal Cracking: high temperatures (typically

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    Cyclohexanol Aim: To prepare an alkene‚ cyclohexene‚ by the dehydration of an alcohol‚ cyclohexanol‚ and better understand the processes that take place during this reaction. Introduction: One of the common ways of preparing an alkene is through the dehydration of an alcohol. In this experiment cyclohexanol is dehydrated to prepare cyclohexene while using sulfuric acid as a catalyst. A bromine test can be later done to ensure that the end product is an alkene. Procedure: The procedure

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    Aniline Synthesis

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    Abstract – This multi-step synthesis uses aniline as the starting reagent to synthesize five compounds employing several reactions such as acetylation‚ diazo coupling‚ nitration‚ bromination‚ and hydrolysis. The isolated products were analyzed with TLC and spectral data that determined most products were pure while some had a few impurities indicated by GC‚ LC‚ and a wide melting point range was shown for products 2 and 3. The presence of water in product 2 and 7 was indicated by the IR. Acetanilide

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    Wittig Reaction

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    The reason it is able to react with the Maleate alkene is due to the presence of the ester groups. these groups are allowing the maleate to resonate and pull the electrons from the alkene towards the esters creating partial positive charges on the carbons of the carbon-carbon double bonds formed next to the carbon-oxygen bonds. Pbu3 can attack these partial positive

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    Detergent

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    DCITATION: http://www.epa.gov/dfe/pubs/laundry/techfact/keychar.htm Surfactants  * Positive Environmental Characteristic: Biodegrade readily to compounds with low toxicity. Example: Straight carbon chain compounds like linear alcohol ethoxylates or betaine esters. * Key Characteristics of Concern: Toxicity to aquatic organisms‚ like fish (vertebrates)‚ daphnids (invertebrates) and algae; persistence in the environment; toxicity of biodegradation byproducts. * Example: Alkylphenol ethoxylates--biodegrade

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    Organic Chemistry

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    Chapter 1 MULTIPLE CHOICE QUESTIONS Topic: Atomic Orbitals 1. A) B) C) D) E) In quantum mechanics a node (nodal surface or plane) is: a place where Ψ is negative. a place where Ψ is positive. a place where Ψ = 0. a place where Ψ2 is large. a place where Ψ2 is negative. Ans: C Topic: Atomic Orbitals‚ Molecular Orbitals 2. When the 1s orbitals of two hydrogen atoms combine to form a hydrogen molecule‚ how many molecular orbitals are formed? A) 1 B) 2 C) 3 D) 4 E) 5 Ans:

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    Physical properties of organic compound Low boiling point group: alkane‚ alkene‚ alkyne and ether Boiling point is the exact temperature that the state of compound change from liquid to gas‚ which need to break the intermolecular forces. The stronger the intermolecular forces‚ the higher the boiling point. Since straight chain alkane‚ alkene and alkyne only experience dispersion forces‚ the compound with more carbons have higher boiling point as more carbons contribute more forces. Branched

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