Step 4: Complete the structure and draw curved arrows. Select Draw Templates C H Cl More :0: : 0 : - :: H Erase Х. Q2Q -(CH3)3COH, -CI¯ Step 2: Addition of ethyl bromide. Complete the structure and draw curved arrows. Select G จ Draw Templates More C H Br : 0: : 0 : : 0 : Erase Br Q 2Q -CH3CH2OH, -Br¯
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- Pls help ASAP. Pls do all asked questions.Use the molecule show and draw the major products using the reagentsPQ-2. This reaction is classified as (A) a nucleophilic addition. (C) a nucleophilic substitution. NaCN H3C CH3 H₂O (B) an electrophilic addition. (D) an electrophilic substitution. HO H3C CN CH3
- What type of alkene is Compound X? (Use all reaction information to solve for Compound X's structure.)3. How would you separate these to compounds using acid-base chemistry? (a) Identify all functional groups; and (b) Draw a flow diagram of your separation process. H3N HOB1) Draw all the Resonance structures for Cycloheptatrienyl anion, using arrows show the flow of electrons (delocalization) in each resonance structure.
- PGF2α (Section 4.15) is synthesized in cells using a cyclooxygenase enzyme that catalyzes a multistep radical pathway. Two steps in the pathway are depicted in the accompanying equations. (a) Draw in curved arrows to illustrate how C is converted to D in Step [1]. (b) Identify Y, the product of Step [2], using the curved arrows that are drawn on compound D.Part G Give the IUPAC name for compound shown below. Spell out the full name of the compound. 2-methylheptanoic acid Submit Previous Answers Request Answer X Incorrect; Try Again Part H CH3 HC-CH2-CH-CH2-CH2-CH2-COOH OH CH3 CH3 -CH2-COOH Give the IUPAC name for compound shown below. Spell out the full name of the compound. HỌC CH–CH HC Submit Previous Answers Request Answer × Incorrect; Try Again5) Use compounds X, Y and Z (shown below) to answer the following questions. H. H3C" "CH3 ОН CH3 compound X compound Y compound Z a) Is compound X classified as cis, trans or neither? b) Is compound Y classified as E, Z or neither? c) Is compound Z classified as R, S or neither? d) Are compounds X and Y constitutional isomers of each other? (YES or NO) e) Are compounds Y and Z constitutional isomers of each other? (YES or NO) f) Classify compound Y as a primary, secondary or tertiary alcohol. g) Which compound(s) is(are) chiral? h) Give the IUPAC name for compound Z, omitting the absolute configuration (R or S) designation. i) In the indicated spaces below, draw stereoisomers of compounds X, Y and Z. stereoisomer of compound X stereoisomer of compound Y stereoisomer of compound Z