デジタル形式で段階的に解決 ありがとう!! SOLVE STEP BY STEP IN DIGITAL FORMAT From the name of the reaction, perform -Your EQUATION (REAGENTS AND PRODUCTS) -Reaction mechanism (EXPLAIN IT STEP BY STEP) a) Antimarkovnikov Hydrogenation b) Antimarkovnikov hydrohalogenation
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- With the molecular formula C4H8O , I ask you to draw 3 molecules: an aldehyde, a ketone and an enol.For each molecule, you must: a) Complete detailed Lewis structure;b) Make the 3D structure respecting the connection angles;c) Determine which intermolecular interactions are present if you glue 2 twin molecules together (2 aldehydes together, 2 ketones together, 2 enols together, therefore 3 situations to analyze).4 For the molecules listed below, tell whether they are saturated or unsaturated and give the shorthand nomenclature. JOD DO OTO (a) Lauric acid (b) Oleic acid (0) 0 (c) Linolenic acid 2odead oals ai 90015 tod (d) Myristic acid mmelini-ions ried to awood read 18 ► 19 20A certain hydrocarbon had the molecular formula C18H30 and contained two triple bonds. Ozonolysis gave CH₂(CH₂)CO₂H and HO₂CCH₂CH₂CO₂H as the only products. Draw a reasonable structure for this hydrocarbon. Click and drag to start drawing a structure.
- Q2/ Attend the following vehicles 1-2-methylbutane from 2-chloro-2-methylbutane 2- butane from ethylchloride (sallOa) 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…The molecule below is a metabolic precursor of both testosterone and estrone. What functional group(s) are present? A) Ketone CH3 B) Aldehyde CH3 H. C) Ether D) Ester E) Ether and ester 0日 PType here to search DELL でu ||||I
- Can you tell me the nomenclature. Thank you in advance.Draw the principal products of thë föllowing reactio (a) H. H CH2CH2CH3 O2 H,CH,C Br (b) NBS hv, CCI4 (c) H2Oing the reactants of products of amidation What is the missing reactant in this organic reaction? ་་་ R + NH2 N. + H₂O H O Specifically, in the drawing area below draw the skeletal ("line") structure of R. If there is more than one reasonable answer, you can draw any one of them. If there is no reasonal drawing area. Note for advanced students: you may assume no products other than those shown above are formed Explanation Check Click and drag to start drawing a structure. ㅁ X
- Alkoxides R-O- can be used to synthesize alkenes as exemplified by the reaction shov below, where the symbol (et) indicates that the substance is dissolved in ethanol (CH;CH,OH) used as solvent: Br (1) + HO Br(et) (et) + (et) CH,CH,OH t-but-Br Ethoxide Isobutylene 9. The table to the right shows the results for the initial rate of this reaction when performed under different conditions (four different trials) at 25 °C. What is the rate law for this reaction? a) Rate = k [t-but-Br] b) Rate = k [t-but-Br] [ethoxide] c) Rate = k [t-but-Br]? d) Rate = k [ethoxide]? Trial Initial Initial Initial Rate (M/s) [t-but-Br] [Ethoxide] [isobutylene] 1 0.08 M 0.04 M 6.8 x 10-8 13.6 x 10-8 6.8 x 10-8 13.6 х 10-8 2 0.16 M 0.04 M 3 0.08 M 0.08 M 4 0.16 M 0.08 MIt is a type of organic reaction in which parts from two molecules exchange. * Elimination Substitution Addition Rearrangement In the reaction given below, what type of addition reaction is used? * H H H H H-C-c=C HBr н-с — с — С —с —н + H H H Br H O Hydrogenation O Hydrohalogenation O Halogenation O Dehalogenation H-O-IIndustrial chemistry: Provide a mechanism for the hydrocracking of n-Heptane in the presence of hydrogen gas to isopentane and ethane.