I Draw the major elimination and substitution products formed in this reaction. Use a dash or wedge bond to indicate the stereochemistry of substituents on asymmetric centers, where applicable. Ignore any inorganic byproducts. Br Q H2O heat Draw One of I the Major Products ■ Draw One of the Major Products ■ Draw One of 1 the Major Products
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- 6. Complete reaction scheme below indicating reagents, catalysts and conditions, and side product trigil bezinslog si6101fon 290b 1l (b Senines levirba 6 gaubong nasamots gniwollot ads to doinW 01 sniowl (6 CH3 40 CH3 Scansgowi (d Ege nodie) ( nsgyxo (b NO₂ 19m02 2i gniwollet sits to mainW II HODraw the structure that dictates absolutely the product of this stereospecific reaction: Br H. CH3 Br Br2 H3C H. H. H3C H3CPredict the major products of the following reaction. Be sure to use wedge and dash bonds to show the stereochemistry of the products when it's important, for example to distinguish between two different major products.
- In both examples below the reactants shown are combined to bring about a nucleophilic substitution (SN1, SN2) and/or elimination (E1, E2) reaction. What is the major reaction that takes place in each case? BrCH₂COCH3 CH3 CH3CH₂CCH3 NaCN CH3OH H₂O SN2 MWhich is true of a free energy diagram for an SN1 eaction? It shows one transition state. It always shows that the reaction is net exothermic. It never shows intermediates. It always shows that the reaction is net endothermic. It always includes multiple energy barriers.Draw the missing reactants/ intermediates in this E1 mechanism. Include all lone pairs. Ignore byproducts.Ignore stereochemistry. I H3O+ : OH H+ Select to I Draw I I Intermediate heat dissociation Select to Draw Intermediate elimination Q Q 1,2-hydride shift I I I I I I I I I
- What is(are) the major final product(s) formed during the following sequence of reactions? 01 11 V 1.0₂ 2. (CH₂)₂S C₂H₂O 2 identical molecules ||| =PPhy < IV орнаWhat is (are) the major organic product(s) obtained from the following reaction? Br2 O (2R,3R)-dibromobutane meso-2,3-dibromobutane O (2S,3S)-dibromobutane O Racemic mixtureStep 4a: Classify step. The target product is present, but the reaction is not over. The ethoxide ion has been regenerated. :0: :0: What is the key process in the next step of the mechanism? proton transfer formation of a o bond between nucleophile and electrophile loss of a leaving group carbocation rearrangement (e.g., methyl or hydride shift)
- Draw the major organic product of the reaction shown below. -OH 3) K₂Cr₂O7 H₂SO4, H₂O You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • In cases where there is more than one answer, just draw one. Ⓒ Sn [F ? ChemDoodleⓇ 6aDraw the major organic product of the reaction shown below. HO NazCr207 H2SO4, H20 H3C CH3 • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • In cases where there is more than one answer, just draw one. C opy aste ChemDoodleWhich of the given compound is most reactive towards E2 elimination? CI H3C, ICH3 H3C CI H3C CI H3C "CH3 H3C CH3 CI H3C