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- Complete each Lewis structure, draw all important resonance structures, predict a value for thebond angles requested, and explain your reasoning. a. Nitrous acid (HNO2)HONOHON=ONO= b. Enolate ion (C2H3O) HC1C2=HC2C1=Rank the indicated a-H’s from most to least acidic (most acidic= 1). Be sure to explain your rankings for each by drawing significant resonance structures for the conjugate base and commenting on any other factors that contribute to your rankings.Draw the major organic product of the Bronsted acid-base reaction between the compounds shown below. Include all lone pairs and charges as appropriate. Ignore any counterions. H H :O: :O: H 1 eq. base :O: H H
- Draw the major organic product of the Bronsted acid-base reaction. Include all lone pairs and charges as appropriate. Ignore any counterions. I :O: NaOH :O: Select to Draw HDraw the organic product of the Bronsted acid-base reaction between the compounds shown below. Include all lone pairs and charges as appropriate. Ignore any counterions. :O: Drawing ÄDraw the organic product of the Bronsted acid-base reaction between the compounds shown below. Include all lone pairs and charges as appropriate. Ignore any counterions. •H :F: :O: :O: H Na Ⓒ 0:0- H
- Q. Explain why Azole undergoes electrophilic substitution at position 2What is the correct statement that links acidity to anion stability? A = CH3 CH2 O H B = CH3 CH2 NH2Draw the organic product of the Bronsted acid-base reaction between the compounds shown below. Include all lone pairs and charges as appropriate. Ignore any counterions. :O: ( H H
- FO 18: Identify resonance contributors. Circle any/all of the resonance contributors for this structure:What would be found in an HNMR of this compound? N- O :ODraw the major organic product of the Bronsted acid-base reaction. Include all lone pairs and charges as appropriate. Ignore any counterions. NaNH2 :O: Select to Draw H