Draw the major product of this reaction. Use a dash or wedge bond to indicate the stereochemistry of substituents on asymmetric centers, where applicable. Ignore inorganic byproducts and CO2. 1. 03 2. Zn, HOAC +
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- Draw the major product from this reaction. Use a dash and/or wedge bond to indicate the stereochemistry of substituents on asymmetric centers, where applicable. Ignore acid byproduct. 1. Br2, H₂O 2. NaH Drawing Q3. Please write out the products or reagents (Note: stereochemistry) H3C Br2 H3C Br2/H2O (2) "a H3C (1) H3C Br2 ( Note: anti-stereochemistry) (3) BrCI H H3C C=C H H H2 (5) (Note: syn-stereochemistry ) Pd/C CH3up an example (not appearing in this ChemActivity) of a pair of molecules that are a)constitutional isomers, b) conformers. c) configurational stereoisomers.
- Draw the major product of this reaction. Include stereochemistry if applicable. Use a dash or wedge bond to indicate the stereochemistry of substituents on asymmetric centers, where applicable. Ignore byproducts. Br H₂OStereochemistry The alkyl bromide below can undergo an E2 but not in its shown conformation. Draw the conformer (as a line drawing, not a Newman projection) out of which an E2 elimination can occur, with all bonds/groups in the original drawing included. 'Bu = tert-butyl H3C H H3C Br tBu alkyl bromide (b) Draw the alkene formed in the E2 elimination reaction of this alkyl bromide promoted by potassium tert-butoxide (KOtBu). (c) Indicate if this E2 elimination reaction is stereospecific or stereoselective (write or circle stereospecific or stereoselective) Regioselectivity (d) Two potential products can form in the following E2 elimination promoted by KOtBu. Circle the major alkene product. (e) KOtBu H3C H3C Indicate if the reaction in (d) is under kinetic control or thermodynamic control. (write or circle kinetic or thermodynamic control) 5Draw the structures for (Z)-3-methylhex-3-ene and the two major organic products for its reaction with HBr. Be sure to show all stereoisomers using wedge and dash stereochemistry at any chirality center.
- below and input the InChl Key string for its structure. To generate an InChI Key from a molecular structure, see these instructions. Consider stereochemistry and enter either enantiomer (but not both) if a racemic mixture of products forms. If the reactants will not react with one another, enter N/A exactly. =0 NH3 (excess), A:&:$:$;$$;$&:&Draw the skeletal (line-bond) structure of trans-1-methoxy-2-methylcyclohexane. Use a dash or wedge bond to indicate relative orientation of substituents on ring where applicable. Draw the skeletal (line-bond) structure of (S)-1-ethoxy-2-methylhexane. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, where applicable. Draw the two starting materials that could be used to make the product via a Williamson ether synthesis.