2. Indicate if the following atoms or bonds are nucleophile (Nu), electrophiles (E) or neither (ne)....
9. Which of the following statements is FALSE of electrophiles and nucleophiles? A) Anionic molecules tend to be nuclophiles, and cationic molecules tend to be electrophiles B) It is possible for the same molecule to act as an electrophile in some reactions, and a nucleophile in other reactions C) Carbocations are very strong electrophiles D) It is possible for a weak nuclophile to participate in a reaction E) Typically, a double headed curved arrow will move towards a nucleophile 10....
I can't figure out where the nucleophile (NU),
electrophile (E), and Leaving group (LG) would go in the
highlighted parts. I've tried multiple different ways.
WB H-0% 2 E
write condensed electron configurations for the following
atoms and indicate the number of valence electrons
2. Write condensed electron configurations for the following atoms and indicate the numbe valence electrons 3. What is wrong with the following electron configurations for atoms in their ground states? (rewrite each one correctly) 1s²2s²3s [Ne]2s²2p3
Which of the following statements is incorrect description of electrophiles? Question 1 options: Electrophiles contain large electron density. Combination of nitric acid and sulfuric acid can generate a strong electrophile. Electrophiles lack electron density. Electrophiles are attracted to negatively charged atoms. Question 2 (1 point) 3-Nitro methyl benzoate is more reactive toward electrophilic aromatic substitution reactions than methyl benzoate. Question 2 options: True False Question 3 (1 point) Predict the carbon atom that carries greatest partial negative charge.
The 2-pyridone anion is an ambident nucleophile. Due to resonance effects, both the carbon and nitrogen atoms are nucleophilic. The nitrogen atom is generally more reactive toward electrophiles, but in the presence of Ag the oxygen atom becomes more reactive. (a) Draw the products of these two reactions in acetonitrile (CH3CN, polar aprotic solvent) (0.4 pts) Ag (b) Why is the nitrogen atom generally more reactive toward electrophiles? (0.2 pts) (c) How do you think Ag' is involved in controlling...
CHSCH HO Draw the molecule on the carwas by choosing buttons from the Tools for bonds. Atoms, and Advanced Template for where needed. The single bond is active by default. including charges E 5C 8 8 8, H 2 0 0 Marvin JS entert @ BOBO Z RYUTOPIA return command option Loooooood Submit Request Answer Part D Of the reactants in Part C, which is the electrophile and which is the nucleophile? CH,COCH, is the electrophile; OH is the nucleophile....
3. For the following reactions, label the reactants as electrophiles (E) or nucleophiles (N). (2 marks) og modo NaOH v Br - V on NaBr
1)Draw the mechanism for Nucleophilic Acyl
Substitution of an acid chloride and a nucleophile
(Nu:-). Be sure to draw all starting
materials, products, intermediate, and curved arrows necessary to
describe this mechanism.(include all arrows and electron
movements)
2)
What is the major organic product for the following reactions? 1. NaCN/H20 2. H30* (heat) N
Check which of the following statements are TRUE. A. Ketones are more reactive as electrophiles than aldehydes. B. One method of shifting the equilibrium in the direction of the ester, in the Fischer esterification reaction, is to remove water as it is formed. C. Methoxy benzene is an activator AND a meta-director D. The following sequence will result in formation of a ketone 1. RCOCl, Ph2CuLi 2. H3O+ E. When a ketone is reacted with LDA (iPr2NLi), the LDA is...
17. For each of the following alkenes indicate whether the molecule is E, Z, or neither. (10pts) Но Но CHз Н CHз CHз Br Hас F F CHз Hас