Here is the question Here is the answer Please explain how to do CH 2. HaO...
please don't copy and paste the answer from other question on
here
QUESTION 3 The IUPAC name of this compound is: Br C=CH-CECH NEC-CH CH2CH2CH3 QUESTION 1 The IUPAC name of this compound is: 0 BICH-CH-CH-CH=CH-C CH,CHE C=0 cí QUESTION 2 The IUPAC name of this compound is: 0- HOCH2CH2CH2
2. For the set of molecules shown circle the strongest acid and explain your selection. FH,CH,CH,CH,CH, C OH H2CH2CH2CH,C(F)HCOH HCHC(F)HCH,CH, COH 3. For the set of molecules shown circle the strongest acid and explain your selection, OP F₃CH₂ cse HẠCHỤC H3CH2C- 20% 3CH₂C-5-00
Please help by showing how to
do the synthesis for both target molecules! Thank you and please be
very thorough with explaining the solvents used and please also
provide a retrosynthetic anaylsis with the forward anaylsis.
Thanks!
7. (16 pts) Synthesize the target molecules using only the carbon sources provided and any reagents of your choosing. Target Molecules Carbon Sources Br Br HO CH3 CH
Predict the products for the following resctions. - Please explain
how you know as I am struggling with the mechanisms if the
reactions are not E2 or Sn2.
5) Predict the products for the following reactions. Do 8 of 9, one will be extra credit. (34 points) Me;coº CH,CH OH 06 H₂ CH3CH2OH
QUESTION 16 10 points Save Answer What is the IUPAC name for the organic product formed in the reaction shown? (no extra spaces) 100℃ CH3-C-OH CH3-NH CH2 CH3 QUESTION 17 10 points Save Answer The "parent molecules for the compound shown are: (select all that appyl) 0 CH3 O phenolic acid benzoic acid QUESTION 18 10 points Save Answer What are the organic compounds produced from the following reaction? (select all that apply) Heat HCI ethanammonium chloride Opropanoic acid sodium...
Can you please answer all of them?
Section B: Free Response (you must show your work for full credit) 1. Draw Frost circle diagrams for each compound shown. Assume that all atoms in the ring are sp2 hybridized. Populate the pi electrons in the corresponding MO's. Identify the compound as aromatic or antiaromatic. (5 pts) 2. What is the Hückel number of pi electrons for the molecule shown below? How many pi electron pairs does it have? Would you expect...
Question 19 (2 points) How many signals would you expect in the 'H NMR spectrum of the following compound? O a) 4 Ob) 5 O c) 6 d) 7 Question 20 (2 points) A compound with a molecular formula of C10H1202 has the following TH NMR spectrum. Which of the following structures is consistent with this spectrum? It til OCH,CH,CH o CH2CH2CHE 11 OH OH CH2CH2CH3 CH2CH2CH3 III IV O a) 1 Ob) III Oc) Od) IV
how do i know which Hydrogens i affect? what do i do here? can
someone explain what im supposed to be looking for with drawings
too? i thought this was an aldol condensation but this says its a
michael reaction and the answer is C. thank you so much!
290. Predict the product: CH2=CH-C + OH CH=CH-C°. CH-&-CH2-8-CzHs Hot H2O H O=0 -C-C-C2H5 о но No reaction: base is too weak to allow deprontonation. CH2 e) C2H5-C-C-C-C2H5 CH2 HG он...
please answer each in 2-3 sentences. thank you
1. We have learned that energy can exist in two primary forms: potential energy and kinetic energy a. Which of the two molecules below contains less potential energy? How do you know? (4 points) CH,OH CH OH —0 OH он H-C-H OH OH b. Glucose is high in potential energy. Why does the cell not simply use glucose to power cellular processes? (2 points) c. Explain how the hydrolysis of ATP can...
Please explain how you got the answer
What are the products implied by the two different mechanistic pathways shown here? PATHWAYA CHCH, - PATHWAY B A + B HECH CHCH CH снен TIT [B] A is II: B is! [E] A is III: B is IV [C] A is l; B is III [A] A is II: B is III [D] A is 1. Bis IV Explanation for your choice (4 pts) Which of these "curved arrows" describe a mechanism...