Which would be the major isolated organic product of the reaction shown? Na, NH3 (1) A) An alkane with an arene attached B) A cis- alkene C) A trans- alkene D) An alkene that is neither cis- nor trans- E) a different product or a mixture of more than one of the choices in equal amounts

Chemistry

Draw the structural formula for the product formed upon hydroboration/oxidation of the Alkene below.

Draw a structural formula for the major organic product of the following reaction: -CH=CH₂ + Br₂ ***** • Show product stereochemistry IF the reactant alkene has both carbons of the double bond within a ring. • Do not show stereochemistry in other cases. • If enantiomers are formed, just draw one. Sn [1 CH₂Cl₂ ChemDoodle Previous Next

Draw a structural formula for the substitution product of the reaction shown below. H3C CI CH3OH • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • If more than one stereoisomer of product is formed, draw both. • Separate multiple products using the + sign from the drop-down menu.

Question 6 Give the major organic product for the following reaction. HgS0, CH3(CH,);C=CH O Cyclohexane 2-Hexanone O Cyclopentanol O Hexanal O Hexanol

The reaction of propan-2-ol in the following series of reactions will yield __________. 1)  NaH; then set aside until Step 3; 2)  CH4 plus Br2, light and heat, assume monobromination; 3) the product of Step 1 mixed with the product of Step 2     an alkene       an alkoxide      an acetylide     an ether     an alkyl bromide

Chemistry the question numbers are in the top left corner of each picture. some questions have more than one picture. thanks!!!

3. Draw structural formulas for the major product(s) resulting from the following reactions: OH Cl2 (a) FeCl3 CH3 .CH3 KMNO4, H* Heat (b) Он (c) Br2

Question 2 Which statement is consistent with the Hammond postulate? O the transition state of an endothermic reaction step structurally resembles the reactant. O it is used to assign the E/Z stereochemistry of alkenes. the less stable carbocation intermediate is formed in electrophilic additions to alkenes. O in additions of HX to alkenes, the H adds to the less substituted alkene carbon and the X adds to the more substituted alkene carbon. O the transition state of an exothermic reaction step structurally resembles the reactant. A Moving to another question will save this response. 80 F3 54 $ 4 000 000 F4 % 5 F5 6 MacBook Air F6 & 7 ao F7 8 DII F8 ( 9 F9