Q2. Rank the following benzoic acid derivatives in order of their pk, values, and explain your reasoning. COOH ÇOOH ÇOOH ÇOOH соон NO2 `NH2 NO2 NH2

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A: There are two possible resonance drawings of methylvinyl ketone.

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Q: ntify whether the following molecules are aromatic, antiaromatic or non-aromati b) c) d)

A: The following molecules are: a) - antiaromatic

Q: 1. Draw a complete, arrow-pushing mechanism that shows the product from each of the following…

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Q: N° N- diazepam w all of the expected products when this compound is completely hydrolyzed in strong…

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A: The given information shows that the 2,3 dibromoethane reacts with 2 equivalents of a base to give 3…

Q: Each nitrogen in the compound below has been given a label A-E. Complete the statements below by…

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Q: Please identify the electrophilic center/s and explain briefly why it is the electrophilic center/s

A: Jjaj

Q: Briefly, but clearly, explain why the –OH hydrogen in acetic acid (CH3CO2H) is more acidic than in…

A: Interpretation - To explain the -OH hydrogen in acetic acid is more acidic than in ethanol.

Q: H. This transformation can be performed with some reagent or combination of the reagents listed…

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Q: How would you synthesize the following compounds from butanoic acid using reagents from the table?…

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Q: + Ph3P. or (E)-3-Hexen-2-one (Z)-3-Hexen-2-one

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Q: true or false of these three potential leaving groups (-OH, -Br , and -OCH3) , -OH is the poorest.

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Q: 2. a. Rank molecules A-D (1 = lowest, 4 = highest) in order of increasing boiling %3D point. Briefly…

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Q: Which one of the compounds below is a Michael donor?

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Q: Which position(s) on the ring will be most likely to be sulfonated? Explain your reasoning for…

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Q: CH, CH, THF/H;0 -: + Hc--CH, CH, + CH, CH, CH Use curved arrows to write the first step of this…

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Q: Which molecule would you predict to be more acidic - propane or acetonitrile? Explain why using a…

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Q: For each of the following substituted benzenes: [1] C6H5Br; [2] C6H5CN; [3] C6H5OCOCH3:a. Does the…

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Q: Which of the following Nitrogens circled in the molecule Ranitidine is the most basic?

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Q: 1. BH3 THF 2. H₂O2/NaOH/H₂O ●

A:

Q: 2. Write the correct IUPAC names for the following organic compounds: A. Br (Assign E or Z…

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Q: Draw curved arrow(s) that depict electron reorganization for the acid base reaction Arrow-pushing…

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Q: Determine the number of stereogenic centers in the compound below.

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Q: If this molecule were exposed to one equivalent oi strong acid, to which carbon would the proton mos…

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Q: Phenols generally have lower pK, values than aliphatic alcohols owing to phenoxide ion stabilization…

A: The answer is given as follows

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Q: Answer both of the following questions precisely, succinctly, and with correct grammar. A. Explain…

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Q: Based on benzene Chemistry, which of the following compounds will direct further incoming group to…

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Q: Classify substituents according to their effect on an SEA by completing the chart below. It is…

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Q: 2) Show an acceptable mechanism for the following transformation using proper curved arrows. I1,0

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Q: 2. Reactivity of Aldehydes and Ketones a. Rank the following aldehydes and ketones in order from…

A: Given: Aldehydes and ketones : A, B, C, & D. The increasing order of reactivity is as follows:

Q: Click on all the electrophiles, then check your answer. : CH3 H,C-C-OH H3C CH3 H2C CH CH3 H. CH3 CH2…

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A: As per the Hammett equation, logkk0=σρ                          (1)   where, σ: Substituent…

Q: Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing…

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Q: On your answer sheet below the answers to the prior problems, draw the major organic product(s) of…

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Q: Provide a plausible arrow pushing mechanism for the reaction below. Note that the starting material…

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Q: Provide a plausible arrow pushing mechanism for the reaction below. Note that the starting material…

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Q: Rank the following compounds in order of decreasing SN1 reactivity?

A: carbocation intermediate stability order :  3°>2°>1°