Write major products, make sure product is the regioisomer and the stereoisomer. Using resonance, explain why the regioisomer that is formed is preferred.
Write major products, make sure product is the regioisomer and the stereoisomer. Using resonance, explain why...
8.42 Addition of HCl to 1-methoxycyclohexene yields 1-chloro-1-meth cyclohexane as the sole product. Use resonance structures to ex why none of the other regioisomer is formed. Cl OCH3 OCH3 HCI
5. which regioisomer will be the major product in reaction in question #4? Explain the reason behind regioselectivity in no more than 3 sentences CI AlCl3
are these correct? if not, can you explain? thanks! Synthesis Reactions: Draw the major products for the following reactions (need not show any byproducts). (3 points each, 21 points) Note: For Diels-Alder reactions, be sure to show relative stereochemistry, if appropriate. atz CH3 1111 CH₂ (be sure to specify the CN product stereochemistry) CN CH2-CH₂-CH₃ SO3, H2SO4 + a. ILICN 30개 Br OCHz AICI: (show monosub. only) - CH₂ CH CH₃ OCH3 H₂ - CH₂ - CH₂ CH₂ - CH₂...
Predict the products of the following reactions. In cases where a stereoisomer is shown, show which stereo isomer(s) are present in the product ارد c=cn New NHl, | PWr: 00 HAR H Fill in the blank 人 A Give all resonance structures for the following Show how they interconvert using the curved arrow notation.
Please predict the ortho/para products, including major and minor. (Write major/minor beside your products) Also, explain briefly why you would expect one product to be major and one to be minor. HNO3 H2SO4 predicted products compound in brown bottle
Find all expected products of this reaction. Predict major product of this reaction and briefly explain why that is the major product. experiment to make an alkene from an alcohol by acid-catalyzed dehydration. OH acid Alkene products heat
Q.Q. Draw the major product(s) for the nitration of the following substrates OOH OCH3 NH2 CN CH2CH3 Q. Which of the following compounds will be in the ether layer after the addition of sodium hydroxide and why? None of the previous NaOH doesn't react with organic compounds Q. The structures of glucose and acetominophen are shown below. Using water and ethyl acetate (a typical organic solvent), in which layer are you likely to find the compounds and why? VOOH но...
Which is the MAJOR product of the below reaction? If multiple products are formed in equal abundance, select all that apply. Question 4 2 pts Which is the MAJOR product of the below reaction? If multiple products are formed in equal abundance, select all that apply. OCH3 CH3 HzC7OH CH3 H2SO4 CH₃ CHз OCH o e a 9 D wi NE O CH3 CH3 H₂Ć CH₃ OOCH3 H3C7 CH3 CH3
Write a detailed mechanism leading to the formation of the MAJOR product. Explain why the following product is NOT the major product. Br2 CHOН о ОСН) Br
#1. Using curved arrows to symbolize electrons, write a complete reaction mechanism for the bromination of acetanilide to create the product. Include the resonance structures for any charged, delocalized intermediates that are involved. #2. Why does performing the experiment at 0 degrees Celsius help you identify some of the relative rates of reactivity? #3. Explain why a methyl group is a mildly activating group while a methoxy group is strong activating. #4. Explain why-- NH2 act as an activator and--...