organic chemistry help!!! Consider the pK_a values (for the bolded H) in toe structures below. Explain...
Organic Chemistry 4. Below are two molecules, B and C. Explain the differences in pKa of the two molecules by drawing the conjugate base of molecule C and a resonance structure that would not be found in molecule B. Hint: Draw out the NO2 group. conjugate base of molecule C pKa- 29.5 molecule B NO2 pka= 8.6 molecule C 5. Below is the molecule Abilify, which is a top selling drug that is used to treat schizophrenia, bipolar disorder and...
help plase with this organic chemistry 2 question? Ch:14 Provide the missing reagents and organic structures for the following transformations.
pls help with this organic chemistry question. 10. Consider the aromatic anions below and their linear counterparts. Draw all of the resonance forms each. What patterns emerge? CHE
Need help with this organic chemistry problem please. Need help with this organic chemistry problem please. What s the driving force that leads to the observed product rather than the molecule below?
1. Consider the following pKa values, and provide explanations (verbally and with structures) for the breaks labeled A, B, and C CH3CH2-H 50 CH2-CHCH2-H 43 41 CH2-H 24 19.3 16.7 O2NCH2-H 10.2 CH2-CHO-H 10.5 10 10.0 1. Consider the following pKa values, and provide explanations (verbally and with structures) for the breaks labeled A, B, and C CH3CH2-H 50 CH2-CHCH2-H 43 41 CH2-H 24 19.3 16.7 O2NCH2-H 10.2 CH2-CHO-H 10.5 10 10.0
Consider the figure shown below. What is the pK_a of hydrogen cyanide, HCN? what is the value of TOTCN for the solution depicted in the figure? Is hypoiodous acid, H0I (pK_a = 10.70), a stronger or weaker acid than HCN? Type stronger or weaker, then briefly explain. Which is the stronger base, cyanide (CN^-) or hypoiodite (OI^-)? Type cyanide or hypoiodite, then briefly explain.
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.
Organic chemistry help! please help 27. (ps) For the following reaction (a) (2pts) Circle the major expected product (b) (5pts) Give the detailed mechanism for the formation of the major product. (Include all steps, intermediates, resonance structures, and electron movement arrows.) (c) pts) Explain important factors related to why one product is fowered -=- Na NHI, 1 +
Hello all, I need an expert in organic chemistry to help with this practice question. Please give answer the question below. Please explain your answers for each drug separately. Please I need your honest answer to this question. Thank you. The question is as stated below; Hello all, I need an expert in organic chemistry to help with this practice question. Please give answer the question below. Please explain your answers for each drug separately. Please I need your honest...
Explain why the different positions have different pKa values, using resonance structures. The pka of phenol (C6H5OH) is 10.0. When a nitro group (NO) is attached to the ring, the pka decreases. Explain why the different positions have different pka values, using resonance structures. OH OH OH - ၄ NO, NO₂ 10. 0 pK, = 7 .23 8.35 7.1