Draw reaction mechanism using arrows. Please indicate nucleophile, electrophile, products, show intermediate structure and name (please show which carbon carriers charges if possible), if anti/syn chemistry is involved, please indicate “anti” or “syn” at the end of the reaction equation. Please name the product. Please indicate “follow Markovnikov’s rule” or “not follow Markovnikov’s rule”. (If hydride shift is possible, please consider it and show it in your reaction)
1) pent-1-ene ( or 1-methylcyclohexene) reacts with Br2
Overall reaction is an example for Electrophilic Addition mechanism and br atoms will add on opposite sides of double bond.
Addition of Br2 is Anti.
It is Stereospecific Reaction.
Draw reaction mechanism using arrows. Please indicate nucleophile, electrophile, products, show intermediate structure a...
2. Draw reaction mechanism using arrows. Please indicate nucleophile, electrophile, product intermediate structure and name (please show which carbon carriers charges if possible)," chemistry is involved, please indicate "anti" or "syn" at the end of the reaction equation. Please name the product. Please indicate "follow Markovnikov's rule or not follow Markovnikov's rule". (If hydride shift is possible, please consider it and show it in your reaction) 1-1) Reaction of the following with HBr in electrophilic addition reactions H3PO4 2) pent-1-ene...
Draw reaction mechanism using arrows. Please indicate nucleophile, electrophile, products, show intermediate structure and name (please show which carbon carriers charges if possible), if anti/syn chemistry is involved please indicate “anti” or “syn” at the end of the reaction equation. Please name the product. 53) Reaction of the following with HBr in electrophilic addition reactions Please indicate “follow Markovnikov’s rule” or “not follow Markovnikov’s rule”. (If hydride shift is possible, please consider it and show it in your reaction) yo...
21) 1-Methylcyclopentene reacts with H2O in presence of BH3, H2O2, NaOH,. Draw reaction mechanism using arrows. Please indicate nucleophile, electrophile, products, show intermediate structure and name (please show which carbon carriers charges if possible), if anti/syn chemistry is involved, please indicate “anti” or “syn” at the end of the reaction equation. Please name the product. Please indicate “follow Markovnikov’s rule” or “not follow Markovnikov’s rule”. (If hydride shift is possible, please consider it and show it in your reaction)
Question: hydration of 2,3-Dimethyl-2-butene in presence of H2SO4 or H3PO4. Draw reaction mechanism using arrows. Please indicate nucleophile, electrophile, products, show intermediate structure and name (please show which carbon carriers charges if possible), if anti/syn chemistry is involved, please indicate “anti” or “syn” at the end of the reaction equation. Please name the product. Please indicate “follow Markovnikov’s rule” or “not follow Markovnikov’s rule”. (If hydride shift is possible, please consider it and show it in your reaction)
Question: 1-Methylcyclohexene reacts with NBS and water (additional question for this question: what the full name of NBS is, draw the structure of NBS) Draw reaction mechanism using arrows. Please indicate nucleophile, electrophile, products, show intermediate structure and name (please show which carbon carriers charges if possible), if anti/syn chemistry is involved, please indicate “anti” or “syn” at the end of the reaction equation. Please name the product. Please indicate “follow Markovnikov’s rule” or “not follow Markovnikov’s rule”. (If hydride...
also show the mechanism and curved arrows for each mechanism 2. Predict the products for the reaction between le products for the reaction between Br, as well as Br/H, and the Alkenes listed below. rredict whether each reaction is syn- or anti-, Label the substrate, nucleophile and electrophile in each reaction. Substrate Structure Overall Reaction with Brz (with products) syn- or Overall Reaction with Bry/H20 (with products) anti- 3,3-dimethyl-1-1 butene 1-hexene styrene (phenylethene)
1. Draw the organic products formed in each reaction. Also show electron movement using arrows. Indicate whether it follows MarkovniKov’s rule : Hydroboration-Oxidation of 2-Butyne Hydration of 1-butyne [1] NaNH2 [1] R BH [2] H2O2, HO- 2 HBr H20 H2SO4
3 Draw eAer reaction were complete. Indicate the nucleophile and electrophile in the first step. Hint-there should be three steps, with two arrows in each step the mechanism for the reaction of the alcohol and the anhydride, assuming it occurred after the 6 pts) if 4) Draw the most favorable conformation of the diene starting material. What implication does this have for the energy of the reaction? (2 pts) 5) Cyclopentene could be used in this reaction in place of...
Please explain and show arrows if possible! Thank you! Q1) Identify the nucleophile and electrophile i ction below and label them. (10 poin + H-C + CT 3 points 'О CN 2. 3 points 3. 4 points
PLEASE ANSWER EVERYTHING Using curved arrows, propose a mechanism for the following reaction. In addition, draw in all lone pair of electrons and positive charges that are needed. Finally, label the Lewis acid, Lewis base, nucleophile, and electrophile in each step. acid catalyst Paraldehyde(a sedative and hyptonic agent)