Question: Can someone please draw Lewis Structures of the following:CO2CH3, COCH3, CH2OCH3, C(CH3)3. And teach me how to draw them, like what atom to look at first, etc? Thank you.

2018年10月20日 · Facts I know: 1) More the electron density in benzene ring, the faster the reaction. 2) Lone pair on -OCH3 group undergoes resonance and makes ortho-para positions electron rich, and so does -CH3 by

Question: Predict the product for the following reaction. COCH3 NaBH4/H20 . Show transcribed image text.

COCH3 1. LIAIH4 2. H20 Edit . Show transcribed image text. There are 2 steps to solve this one. Solution ...

Observe that the reaction involves the use of the reducing agent lithium aluminium hydride (LiAlH4) in excess, indicating that all "ketone" and "ester" groups present are expected to undergo reduction.

19. Which of the following sets of substituents are all ortho/para directing in electrophilic aromatic substitution reactions? a. -CI, -CH3, -CN b. -Br ,-OH,-COCH3 -Cl ,-OH,-CH3 c. d. CN, -NO2, -COCH3 20. Which of the following sets of substituents are all deactivating groups in electrophilic aromatic substitution reactions? a. CI, CN, NO2 b.

br, ch3, no2 c. ch3, nh2, br d, no2, coch3, cooh Your solution’s ready to go! Our expert help has broken down your problem into an easy-to-learn solution you can count on.

What type of directing groups are these substituents? Which one is the stronger directing group? N N O Deactivating; -N(CH3)(COCH3) is stronger O Electron Donating; -N(CH3)(COCH3) is stronger O Electron Withdrawing; -N(CH3)2 and -N(CH3)(COCH3) are both equally strong Activating; -N(CH3)2 is stronger Electron Donating; -N(CH3)2 and …

2019年12月1日 · Most people would call it vinyl acetate. If you want the systematic name, then it is ethenyl ethanoate. It is formally derived from "vinyl alcohol" and acetic acid, from which the name follows easily.

COCH3 ester oxide carboxylic acid acid anhydride What is the missing number most likely to be for the ...