(a) A secondary alcohol on reaction with chromic acid (H2CO4) gives a ketone (D).
(b) The ketone D in presence of H2O and H2SO4 gives a diol (F).
(c) The primary alcohol on reaction with pyridinium chloro chromate (PCC, a mild oxidizing agent) gives an aldehyde (H).
(b) This is a Friedel-Crafts acylation reaction. Since Cl is ortho- para directing group and -COCH3 is meta directing the acyl group added in para position of the
-Cl atom. Hence the product is (B).
(5) (9 points) Reactions involving aldehydes and ketones. In the text boxes below, indicate the most...
9. Reactions involving Enolates Ketones E) B-dicarbonyl Aldol: best with aldehydes Aldol addition Hproduct t冫 Aldol condensatiorn product Claisen Reaction: Esters!
9. Reactions involving Enolates Ketones E) B-dicarbonyl Aldol: best with aldehydes Aldol addition Hproduct t冫 Aldol condensatiorn product Claisen Reaction: Esters!
(B) In the boxes below, draw the two self-condensation pro products that result from the mixture in Model 2. Use the roles reagent listed in each box to determine the products. Eation products and two mixed condensation Use the roles (Nu, Ee) for each Self Condensation Nuo = A ΕΦ = A Self Condensation Nuo = B E =B Mixed Condensation NuO = A E = B Mixed Condensation NuO = B ΕΦ = A 5. Mixed condensations can also...
Draw the structures of the product(s) of the six reactions below. Clearly indicate stereochemistry where needed. If a pair of enantiomers results, clearly depict both enantiomers. If you think that there will be no reaction then write: "No Reaction." Racemic Mixture Br2in CCI H2 and Pt H\OTs H3C (C) KCN in DMSO (s,2 Product) KOtBu and Heat in tBuOH CH3 OTs H,C OH 1Tsa in Pyridine 2) KOtBu and Heat in tBuOH CH3 CH CH 0% 2) Excess (CHJ2S
Draw...
This experiment was based on Aldol-dehydration reaction using
unknown aldehydes and ketones. We carried out an aldol condensation
between an unknown aldehyde and an unknown ketone. Here are the
list of possible unknown aldehydes and ketones that were used.
Here is the NMR of the final product. Please predict the
structure given the melting point is 163 degrees Celsius.
The analysis of the 1H NMR spectrum should include a detailed
assignment of each of the NMR resonances to the protons...
3. (21 points) Provide the major product for each reaction below. Be sure to indicate appropriate stereochemistry when relevant ОН HB 90°C Xusuguay Br CH.CH, ONA CH,CH,OH * NaN acetone-water (solvent) 9. H.Co
C. REACTIONS: (8 points each; 40 points total) For each of the following reactions or series of reactions, draw the final major organic product, reactant, or reagents in the box. Be sure to indicate STEREOCHEMISTRY where pertinent. In multiple step reactions, you may place intermediate products below the reaction for partial credit. 1. NH2 2. 1) NBS, hv 2) NaCN 0.5 eq 3) NaOH, H20 4) HCI 3. 1) NaBH4 2) MCPBA 3) NaOH 4) excess acetic acid, H+
5. (25 Points) Draw all products for the following two reactions. Be sure to indicate stereochemistry if it is relevant. Clearly state whether each product came from an E1, SX1, E2, or S2 reaction. NaOME MeOH, heat
super easy points
Aldehydes and Ketones Classify each molecule as an aldehyde, ketone, or neither. Drag the appropriate molecules to their respective bins. Draw the aldehyde produced from the oxidation of CH3CH2CH2C(CH3)2CH2OH. Draw the molecule by placing atoms on the grid and connecting them with bonds. Include all hydrogen atoms. Draw the ketone produced from the oxidation of 2-pentanol. Draw the molecule by placing atoms on the grid and connecting them with bonds. Include all hydrogen atoms. Carboxylic Acids and...
Question 3. Predict the major products of the reactions below. Draw the full mechanism for the reactions, using appropriate arrows to indicate electron movement and the full structures of any intermediate(s). Use the mechanism of the reaction to provide a rationale for why the major product formed. OM (1 equivalent) ansole Bry Febr (1 culle brambenzone Fer (1 equivalent Priloromethylbenzene (9 marks) Question 4. Predict the major product from the treatment of 2,5-dibromopyridine with ammonia. Draw the full mechanism for...
Chapter Exhibit 6-5 Add curved arrows to the following reactions to indicate the flow of electrons in each. = 23. --H + H2C - M9Br - CH + H : MgBx Exhibit 6-9 Use the reaction energy diagram below to answer the following question(s).