Question 3 of 20 (1 pont) X incorrect incorrect × Incorrect X incorrect 2( Incorrect 2e...
14 Question (7 points) e See page 897 Draw the curved arrow mechanism for the formation of an acetal from acidic methanol and pentan-2-one in the fewest steps. When given the choice, draw the arrows that lead to the resonance structures with full octets around each atom other than hydrogen. Do not show any inorganic byproducts or counterions. Reagents needed for each step are provided in the boxes. - وہ : SH : 0I :O- T 0 -ة: I- i...
The first four are correct, I just do not know how to do the
following steps to get the final product (which I also
know)
Draw the curved arrow mechanism for the reaction of 3-methylbutanenitrile and CH3Li, followed by the addition of acid to give the major product in the fewest steps. When given the choice, draw the arrows that lead to resonance structures with full octets around each atom other than hydrogen. Draw all atoms, electrons, and es if...
10 Question (4 points) e See page 890 Draw the curved arrow mechanism for the addition of HCN in water with NaOH to 3,4-dimethylcyclopentan-1-one to give the corresponding cyanohydrin in the fewest steps. Draw the arrows that lead to the resonance structures with full octets around each atom other than hydrogen. Draw all electrons and charges if necessary on all structures; do not show any inorganic side products or counterions. Reagents needed for each step are provided in the boxes....
Question 7 of 21 (1 point) × Incorrect X incorrect Xincorrect ×Incorrect ×Incorrect ×Incorrect- CH3 Did you draw only curved arrows in the first three boxes? Did you draw a structure in the two empty boxes? Do not delete or add any atoms, bonds, or lone pair electrons Does each curved arrow start at an electron-rich atom or bond? Do the structures contain the correct valence, lone pair electrons, and nonzero formal charges? + HOCH2CH3 H3C. C Try Again View...
Need arrows, charges, and mechanistic intermediates how the
boxes specify
Draw the curved arrow mechanism to show the conversion of hex-1-ene and CHyOH in acid solution into 2- methoxyhexane. Follow the instructions under the boxes for each step. Draw all necessary atoms and charges, do not add any structures. Add any necessary atoms and charges to the carbon structures above to show the proper mechanistic intermediates and draw curved arrows to show the next mechanistic steps. Draw aurved arrows above....
When naphthalene undergoes an irreversible electrophilic aromatic substitution, the major product is the kinetic product, which proceeds through the most stable arenium ion intermediate. With this in mind, draw the curved arrow mechanism for the first step of the electrophilic aromatic substitution of naphthalene with l^+ generated from l_2 and CuCl_2. If you predicted the correct regiochemistry in the first step, then you can draw the curved arrows and a resonance structure in step 2 with an unbroken benzenoid ring....
Draw the curved arrow mechanims for the reactions of but-1-yne
with catalytic trifilic acid in water to form butan-2-one,
I just can't seem to figure out the last step! Thank you in
advance!
Draw the curved arrow mechanism for the reaction of but-1-yne with catalytic triflic acid in water to form butan-2-one. Follow the instructions under the boxes for each step. Draw all electrons and charges if necessary on all structures, do not show any inorganic side products Add any...
a See page 1127 13 Question (3 points) When naphthalene undergoes an irreversible electrophilic aromatic substitution, the major product is the kinetic product, which proceeds through the most stable arenium ion intermediate. With this in mind, draw the curved arrow mechanism for the first step of the electrophilic aromatic substitution of naphthalene with the acylium ion generated from acetyl chloride and AlClg, Then draw the curved arrows and a resonance structure in step 2 with an unbroken benzenoid ring.Draw all...
everything is correct except for step 3 i dont know whats
wrong
Hydrolysis of 2-bromo-2-methylpropane (tert-butyl bromide) yields 2-methylpropan-2-ol. (CH),CBr + 2H,0 → (CH),COH + H,0* + Br Give the Sn1 mechanism. The reactants are already given in step 1: you need to start by adding curved arrow(s) to the reactants. For each remaining step, draw all species regardless of if they are involved in that step or not. Also, include electrons and charges where necessary. Details count. Note: You...
please answer and label all steps
Hydrolysis of 2-bromo-2-methylpropane (tert-butyl bromide) yields 2-methylpropan-2-ol. (сн), сон + н,о* + CH CBr 2H,O Br Give the SN1 mechanism. The reactants are already given in step 1; you need to start by adding curved arrow(s) to the reactants. For each remaining step, draw all species regardless of if they are involved in that step or not. Also, include electrons and charges where necessary. Details count Note: You should have 4 carbon atoms, 13...