Is the NO molecule a good electrophile? is it a good nucleophile? or neither? Briefly explain...
Is the NO molecule a good electrophile? is it a good nucleophile? or neither? Briefly explain answer.
Homework Answers
Before answer the question we need to understand what is electrophile and what is nucleophile.
Electrophiles mean the species which likes electrons and these species has shortage of electrons.. They have attraction for electrons and accept electrons whenever possible.
Nucleophiles are the species which are already electron rich and the central atom has filled octet. They like to donate electrons.
Now in nitric oxide (NO), the N atom is electron deficient. It has total seven electrons in it's valence shell. Therefore octet is not filled up. So it will have a tendency to accept electron to fill it's octet. Again oxygen atom is highly electronegative which attracts bond pair electrons towards it and make N atom more electron deficient and partially charged. Therefore it will have attraction for electrons and hence works as electrophile.
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Is the NO molecule a good electrophile? is it a good
nucleophile? or neither? Briefly explain...
Classify each structure below as a nucleophile or electrophile, and briefly explain your choice Identify and...
Classify each structure below as a nucleophile or electrophile, and briefly explain your choice Identify and label the nucleophile and electrophile in each reaction below. Then add curved arrows to indicate the flow of electrons in each.
4. (6pts) Label each molecule as a nucleophile or electrophile AND draw an arrow pointing to...
4. (6pts) Label each molecule as a nucleophile or electrophile AND draw an arrow pointing to the atom on the molecule that would be the nucleophile or electrophile CI CEN HTΉ I verbo on si smith H-C-OH I-O-I H₃C – NH₂ Hool H3CH
For the following reaction, label the nucleophile, electrophile, and leaving group, Br + + Br Nucleophile...
For the following reaction, label the nucleophile, electrophile, and leaving group, Br + + Br Nucleophile Select] Electrophile (Select] Leaving Group [Select] For each of the following pairs, indicate with molecule is the better (stronger) nucleophile. [Select] [ Select] Z-I [Select) [Select]
(14 pts) 2. Define electrophile. Give an example of charged molecule that reacts as an electrophile:...
(14 pts) 2. Define electrophile. Give an example of charged molecule that reacts as an electrophile: Give an example of an electrophile that has a partial charge: Give an example of an electrophile that has no charge: Define nucleophile Give an example of a nucleophile that is charged: Give an example of a nucleophile that has a partial charge: Give an example of a nucleophile that has no charge:
each of the following compounds, identify the reactive sites (strong nucleophile, strong electrophile, good leaving group,...
each of the following compounds, identify the reactive sites (strong nucleophile, strong electrophile, good leaving group, reasonable acid Ipka<201or strong base; many atoms will have no discernable reactivity): NaOCH
sn2, Nucleophile and eclectrophile 9. Consider the SN2 product below. Provide a nucleophile and electrophile the...
sn2, Nucleophile and eclectrophile
9. Consider the SN2 product below. Provide a nucleophile and electrophile the below. Provide a nucleophile and electrophile that, when reacted, would result in the product provided. Multiple correct options exist. (2 points) DY= electrophile nucleophile
Classify each of the following as an electrophile or a nucleophile.
Classify each of the following as an electrophile or a nucleophile.
Nitrate is a a. very good electrophile b. very poor electrophile c. very poor nucleophile d....
Nitrate is a
a. very good electrophile
b. very poor electrophile
c. very poor nucleophile
d. very good nucleophille
ethanol is
a. non-polar aprotic or proatic
b. polar
silver ion will coordinate very efficiently with any free
halide and form a precipitate, promotiong the ionization of
halohydrocarbons and formation of
a. resonance
b. carbocations
c. carbanions
Thus, the AgNO3/ethanol reagent favors reactivity by the
a. SN1
b. SN2
= $ Return Submit 5 points Finish the sentence by filling...
where would the electrophile end up if the following molecule underwent an electrophilic aromatic substitution reaction....
where would the electrophile end up if the following molecule
underwent an electrophilic aromatic substitution reaction.
QUESTION 9a: Where would the electrophile end up if the following molecule underwent an electrophilic aromatic substitution reaction? Briefly explain your reasoning
Molecule: Atenolol Question: 1. Indicate the 1-2 most electrophile site(s) in the molecule. 2. Indicate the...
Molecule: Atenolol
Question:
1. Indicate the 1-2 most electrophile site(s) in the
molecule.
2. Indicate the 1-2 most nucleophile site(s) in the molecule.
olar HN OH
Classify each structure below as a nucleophile or electrophile, and briefly explain your choice Identify and label the nucleophile and electrophile in each reaction below. Then add curved arrows to indicate the flow of electrons in each.
4. (6pts) Label each molecule as a nucleophile or electrophile AND draw an arrow pointing to the atom on the molecule that would be the nucleophile or electrophile CI CEN HTΉ I verbo on si smith H-C-OH I-O-I H₃C – NH₂ Hool H3CH
For the following reaction, label the nucleophile, electrophile, and leaving group, Br + + Br Nucleophile Select] Electrophile (Select] Leaving Group [Select] For each of the following pairs, indicate with molecule is the better (stronger) nucleophile. [Select] [ Select] Z-I [Select) [Select]
(14 pts) 2. Define electrophile. Give an example of charged molecule that reacts as an electrophile: Give an example of an electrophile that has a partial charge: Give an example of an electrophile that has no charge: Define nucleophile Give an example of a nucleophile that is charged: Give an example of a nucleophile that has a partial charge: Give an example of a nucleophile that has no charge:
each of the following compounds, identify the reactive sites (strong nucleophile, strong electrophile, good leaving group, reasonable acid Ipka<201or strong base; many atoms will have no discernable reactivity): NaOCH
sn2, Nucleophile and eclectrophile
9. Consider the SN2 product below. Provide a nucleophile and electrophile the below. Provide a nucleophile and electrophile that, when reacted, would result in the product provided. Multiple correct options exist. (2 points) DY= electrophile nucleophile
Classify each of the following as an electrophile or a nucleophile.
Nitrate is a
a. very good electrophile
b. very poor electrophile
c. very poor nucleophile
d. very good nucleophille
ethanol is
a. non-polar aprotic or proatic
b. polar
silver ion will coordinate very efficiently with any free
halide and form a precipitate, promotiong the ionization of
halohydrocarbons and formation of
a. resonance
b. carbocations
c. carbanions
Thus, the AgNO3/ethanol reagent favors reactivity by the
a. SN1
b. SN2
= $ Return Submit 5 points Finish the sentence by filling...
where would the electrophile end up if the following molecule
underwent an electrophilic aromatic substitution reaction.
QUESTION 9a: Where would the electrophile end up if the following molecule underwent an electrophilic aromatic substitution reaction? Briefly explain your reasoning
Molecule: Atenolol
Question:
1. Indicate the 1-2 most electrophile site(s) in the
molecule.
2. Indicate the 1-2 most nucleophile site(s) in the molecule.
olar HN OH
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