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- On the line drawn below, provide the systematic (IUPAC) name for the following structure. Besure to include stereochemistry (R/S, cis-trans, or E/Z) when appropriateOn the lines drawn below, provide the systematic (IUPAC) names for the followingstructures. Be sure to include stereochemistry (R/S, cis-trans, or E/Z) when appropriate. please show each step.1-methylcyclohexene is reacted with the following reactants. Write products. Write which stereochemistry is valid (syn/anti, racemization, antimarkovnikof, etc). 1- Br2/ H2O 2- CH2N2/heat
- Using any necessary organic and inorganic reagents, show how you can carry out the chemical conversions shwon below. Please answer parts a, b, and c.Bromide Bhas normal activity (for a secondary bromide) towards SN1 substitution, but A has much higher reactivity and Chas much lower reactivity.Five-membered aromatic heterocycles with one heteroatom undergo electrophilic substitutions preferentially at the α-position (C-2 and C-5) rather than at the β-position (C-3 and C-4). Explain?
- Which of the following statements about an -NH2 group is FALSE? a. meta director b. activator towards EAS c. increases electron density on the aromatic ring d. stabilizes positively charged intermediates by resonance or inductive effectsDraw the products formed when both cis- and trans-but-2-ene are treated with OsO4, followed by hydrolysis with NaHSO3 + H2O. Explain how these reactions illustrate that syn dihydroxylation is stereospecific.Provide the mechansim using curved arrows of the reaction of p-t-butyl phenol treated with acetic anhydride in AlCl3. Include resonance stabilized intermediates and if more than one product is formed, label them as major, minor, etc. thank you for the help
- The treatment of isoprene [CH2=C(CH3)CH=CH2] with one equivalent ofmCPBA forms A as the major product. A gives a molecular ion at 84 in itsmass spectrum, and peaks at 2850–3150 cm−1 in its IR spectrum. The 1HNMR spectrum of A is given below. What is the structure of A?Complete the reaction map by providing the answer from A-E. Write the IUPAC name of the products. conc HNO B conc H,SO, B, D FeBrs conc HNO, E AIC conc H2SO. conc H2SO4Electrostatic potential maps of anisole and thioanisole are shown. Which do you think is the stronger acid, p-methoxybenzoic acid or p-(methylthio)benzoic acid? Explain.