Draw a resonance stabilized conjugate base derived from nepetalactone, circle the major resonance contributor or write equal if they're equal, also lable the most acidic hydrogen of the molecule.
Draw a resonance stabilized conjugate base derived from nepetalactone, circle the major resonance contributor or write...
1. Draw all resonance structures for the following compound. Circle the major contributor (to the resonance hybrid) and give a brief explanation for your choice. (4 pts) 2. Determine the configuration (show priorities and work) for any chiral centers in the molecule below. (2 pts) 2. Determine the configuration (show priorities and work) for any chiral centers in the molecule below. (2 pts) 1. Draw all resonance structures for the following compound. Circle the major contributor (to the resonance hybrid)...
There are two resonance contributors for the molecule. Draw the major resonance contributor of the following ion: There are two resonance contributors for the molecule. Draw the major resonance contributor of the following ion:
Draw all major resonance structures of the conjugate base of acetophenone. The most acidic hydrogen atom in acetophenone is drawn in red. Interactive 3D display mode Draw the molecule on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Template toolbars, including charges where needed. The single bond is active by default. Draw a mechanism for this reaction. Interactive 3D display mode Edit the reaction by drawing all steps in the appropriate boxes and connecting them...
Q.1. Draw the conjugate base or conjugate acid of the following species Conjugate Acid Conjugate Base a) OH Sb) ? CH3NH2 c) HO d) ? SO- Q.2. ) Circle the most acidic proton and cross out the least acidic protons among the shown hydrogen atoms in the following molecules. NO H NH2 O-H Η Η CH3 OH -SC-H Н" Q.3. Circle the most acidic compound and cross out the least acidic compound in each set. ou la olagla ОН OH...
5) Draw the conjugate bases of the compounds shown below. Show how each conjugate base is stabilized by delocalization/resonance. H (a) но (b)
6) Draw the conjugate acid of the compound shown below. Show how the conjugate acid is stabilized by delocalization/resonance. 7) Identify the most acidic proton in the molecule below. Use resonance structures to explain your answer. Н,с "Cн, нн
Draw all resonance structures for this molecule and determine the major and minor resonance contributor. Where do you start when there are two groups attached to a benzene ring? :0 CH3
draw resonance structures for the conjugate base of 2,6dichloroibdophenol and use them to explain the differences in the pka values a value of 5.9 and is 10.000 times more 2,6-dichloroindophenol (see in Part III) has a pka value of 5.9 and is 10000 acidic than phenol (pKa =10). Draw resonance structures for the conjugate base of 26 dichloroindophenol and use them to explain the differences in the pKa values.
Consider the reaction of the aldehyde below with a base (Removal of hydrogen to form carbonanion). 1. Draw the conjugate bases for each H removal and, II. Circle the base with an acceptable resonance form.la но Base PIPI III. Draw this resonance form. IV. Which of the two forms is of lower energy This proton removed is of the lowest energy! This is the most acidic proton.
Question 7 Using curved arrows, deprotonate the most acidic hydrogen and draw the conjugate base. The conjugate base is relatively stable due to delocalization. When drawing the curved arrows, illustrate that delocalization which should result in the best contributing structure of the conjugate base. HO with her + H20 Question 10 veten som The reaction scheme below illustrates the addition of H-Br to a double bond. Draw a curved arrow mechanism and the missing intermediate. en die onderkant van den...