The intermediate formed in the previous step is resonance-stabilized. Draw the missing curved arrow(s) to convert the first resonance structure into the second one. Qu Fill :0 H3C H H3C H Edit Drawing Qu Mul Qu Mol Qu Fill in
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- Draw the most stable resonance form for the intermediate in the following electrophilic substitution reaction. CI CI HNO3 / H2SO4 O2N You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. • In cases where there is more than one answer, just draw one.Draw both resonance structures of the most stable carbocation intermediate in the reaction shownDraw the energy diagram for the reaction below showing the transition state (s)
- Question 5 1). Draw all resonance structures for the carbocation intermediate formed by para attack; circle the resonance structure that is particularly unstable. N- N Cl₂ AICI 3 H 2). Draw all resonance structures for the carbocation intermediate formed by ortho attack; circle the extra resonance structure that is particularly stable. H a Aer ANSAS C HNO3 H₂SO4Alkene bromination. The two butane isomers react with Br2. Draw the key reaction inter- mediates and the product(s); use arrow pushing to explain the stereochemical outcomes of the reactions Final Products Intermediate Br2 Intermediate Final Products Br2s sugar X a reducing or a non-reducing sugar? Reducing, because one/both of the rings can open to expose a free aldehyde group Non-reducing, because one/both of the rings can open to expose a free aldehyde group Reducing, because neither of the rings can open to expose a free aldehyde group Non-reducing, because neither of the rings can open to expose a free aldehyde group Reducing, because one/both of the rings can open to expose a free ketone group Non-reducing, because one/both of the rings can open to expose a free ketone group Reducing, because neither of the rings can open to expose a free ketone group Non-reducing, because neither of the rings can open to expose a free ketone group Cannot be determined from the structure shown
- Draw the most stable resonance form for the intermediate in the following electrophilic substitution reaction. _NH2 NH2 Br2 Br • You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. • In cases where there is more than one answer, just draw one.draw an energy diagram that follows the criteria belowWhich of the following describes the reaction whose reaction coordinate diagram is shown below? Free Energy Progress of na endergonic with no transition state exergonic with no transition state endergonic with an intermediate exergonic with a transition state endergonic with a transition state
- The conversion of reactant R to product A is under control and is preferred a temperature kinetic, low kinetic, high thermodynamic, low thermodynamic, high The conversion of reactant R to product B is under control and is preferred at temperature kinetic, low kinetic, high thermodynamic, low thermodynamic, high Electrophilicity is the tendency of a species to accept electrons due to energy orbitals. low, unoccupied low, occupied high, unoccupied high, occupiedWhat carbon radical is formed by homolysis of the C–Hb bond inpropylbenzene? Draw all reasonable resonance structures for thisradical.2. a) b) Ez Draw the products of each / elimination Фоснасня H |||| Br H3 C H Ф OCH₂CH3