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 shift is possible, please consider it and show it in your reaction)
NBS is a selective brominating reagent at allylic and benzylic position by free-radical Substitution.
Question: 1-Methylcyclohexene reacts with NBS and water (additional question for this question: what the full name...
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
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)
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...
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...
4. Explain things in the following question(s) In each reaction, identify the Brønsted-Lowry acid, the Brønsted-Lowry base, the conjugate acid, and the conjugate base. (a) H2SO4(aq) + H2O(l) —— HSO4 (aq) + H30+(aq) (b) HCO3(aq) + H20(1) = H,CO3(aq) + OH(aq) 5. Using examples, distinguish between a Nucleophile vs Electrophile. Give at least 2 differences between the 2 concepts 6. What are curved arrows or "curly arrows" in Organic Chemistry? What do they represent? Give an example (b) Using Ammonia...
1) Draw structures for compounds named below. A) (2)-1-bromo-2-chloro-1-heptene B) 4-chloro-4-fluoro-2-octyne 2) Give IUPAC name for the following structure. 3) For each reaction below, indicate which starting material is the Nucleophile and which is the Electrophile. Show arrows to demonstrate how the transformation occurs. →^_^tts a Porto ~ onde gi 4) Draw a mechanism for the conversion of the shown starting material to the corresponding product. 5) In the transformation below, a starting material is treated with HCl to form...
1.(a) (2pts.) Draw the structural formula for each amine. (b) provide the IUPAC name the structure below 4-aminobutanal (R)-2-butanamine 2. (6 pts.) Consider the Grignard reaction shown below which forms a C-C bond via an Aw step. In box A, draw the structure of the nucleophile involved in the A step and highlight the nucleophilic atom. In box B, draw the structure of the electrophile involved in the Aw" step and circle the electrophilic atom. In box C, draw the...
please Answer in Details showing all the steps. Thank you Look at the following reaction: Toluene OH + CH3OH OCH3 + H2O a) What is the effect of each of the given changes (see next page) on the rate of the reaction? The possible answers are: Increases, decreases, remains the same or no more reaction. 1- Decreasing the concentration of CH,OH 2-Using a Dean-Stark apparatus (used to remove water from the reaction mixture) 3- Adding H,SO, to the reaction mixture...
PLEASE ANSWER ALL QUESTIONS Question 5 The reaction below occurs via SN2 and E2 reaction mechanisms. The question only requires you to address the E2 reaction only. For the E2 reaction: Use Newman projections to show the relationship between the leaving group and the beta-hydrogen on the carbon labeled with the asterisk ("). 1. If the leaving group and the beta-hydrogen on the carbon labeled with the asterisk (1) are not in the correct orientation, show the result of the...