Click on the Pub Chem link below and answer the question below. Pub Chem Sketch Tool a) Provide the StdInChI notation for the intermediate generated after step #1 when 2-methyl-2 -butene is reacted with HBr in an acetic acid solvent. b) Provide the StdInChI notation for the final neutral product. c) Provide the name of the final neutral product.
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- What is the major organic product in the following reaction sequence? Type its systematic IUPAC name in the box below. Br 1) NaCN 2) H3O*, heat ?The ACS exam at the end of this semester covers a limited amount of IUPAC nomenclature mostly from Organic I. An example is given below, what is the IUPAC name of of the compound whose structure is shown in the box? A) E-1- butylidene-1-iodo-propane B) E-5-iodo-4-heptene C) E-1-(1-iodopropylidene)-butane D) E-3-iodo-3-heptene A Вorgo chem questions
- Fill in the missing reactants, reagents, or products. More than one step may be needed to fill the boxes for missing reagents.please help with the following OChem question 1. Provide the bond line structures and the IUPAC names for the major organic products formed in each step of the following reaction scheme (see attached image)12) Use the curved arrow formalism to show the movement of electron pairs in the following reaction and label each reactant as a nucleophile or an electrophile. CHÍNH CHỊCH, + CO Học Nha CH₂CH₂CI
- A) An Alcohol X has the structure of (CH,), C(OH)CH(CH,),. i) State the IUPAC name of alcohol X. i) Outline the mechanism for the reaction occurring when alcohol X is converted into 2,3-dimethylbut-2-ene in the presence of a strong acid. i) Name the reaction in part ii). iv) Draw the structure and state the IUPAC name of an isomer of 2,3-dimethyl-2- butene which is also formed in the reaction. v) Explain why two products are obtained. vi) Write an equation for the reaction between alcohol X and ethanoyl chloride. vii) Outline a mechanism for this reaction, using ROH to represent the alcohol in the mechanism.a) Draw the major product(s) of the following reactions. i) ii) OSO4 NaHSO4, H₂O BH3-THF H₂O₂, NaOH b) Methylcyclohexene reacts with chlorine both in CCl4 and water. i) Draw the structural formula for both the products. > ( )Complete the table below with all the missing information. Note: more than one reactant/reagent/product may be required in a row/column.
- Oa) An amine can be formed when 2-iodopentane is heated with ammonia in a sealed tube. This is an example of a nucleophilic substitution reaction. i) Provide a full equation (using condensed formula) for this reaction. You should name the reactants and the overall products as part of your response. ii) Name the organic product formed from this reaction and draw it's displayed structure. iii) Provide a 'curly arrow' mechanism (in displayed formula) with an accompanying explanation for this process. iv) Describe a characteristic test (with the result that would be observed) to show the presence of the amine produced upon completion of the nucleophilic substitution reaction. b) The amine produced in the above reaction forms a mixture of two optical isomers. i) Draw the 3D structures of the two isomers of the amine product that you named and produced a drawing of in part a ii). ii) With reference to a different named example, explain the term 'optical isomer'. You should draw the 3D…Draw the overall reaction of 2-bromo-2-methylpropane with H2O to give the alcohol product. Include all by-products that form.1. The acid-catalyzed elimination of an alcohol is an equilibrium reaction and requires special reac- tion conditions to favour the formation of the alkene product. What chemical principle controls the amount of alkene product that is produced? Provide two laboratory techniques that can be used to obtain good alkene yields in alcohol elimination reactions.