allyl halides generally undergoes the sn1 , sn2 and e2
reactions only based on the type base the possible products are
formed as follows
Question Two We change the substrate to allyl bromide and things change quite significant what are the products, an...
Question Three We change our substrate to benzyl chloride. What does this substrate have in common with the substrate in Question Two? What key difference does it have that leads to a different outcome in one reaction? H2O H₂O H₃ C CH3
Question 32 1 pts What are the products of the following hydrolysis? CH3-CH -CH-E-N+-CH3 + H2O + HCI снуснған 8-н, сна CHỊCH-CH-Z-OH + CHÚNH,+ C CH=CH=CH22O + CHẠNH, CH3-CH4-CHz-C-OH+CH3NH2
Question 15 Compound A on ozonolysis yields the following two products What is the structure of compound A? Compound A 1.03 2. (CH3)2s IV
9) What are we removing with the water wash? Why don’t we just add the sodium bicarbonate directly to the reaction mixture instead of doing a water wash? 10) Provide the results of the silver nitrate test. Introduction Alkyl halides can be prepared from alcohols by reactions with hydrogen halides (HCl, HBr, or HI) via nucleophilic substitution. In this type of reaction, the nucleophile displaces a leaving group from a carbon atom of an organic substrate (here the alcohol once...
What are the products for the two step reaction? Question com Question 18 What are the products for to reaction below را .1 ميn A هر 2 الري" " راه h .COM . B Type here to search 0
Jame: . Complete this mechanism for the following substitution reaction. Note: this reaction is balanced. H-Br Н,0 OH -CH3 H20 Step 1: proton transfer Step 2: lose water Step 3: attack the carbocation Br -CH3 . Each reaction above is reversible. In question 1, what effect would adding more HBr have on the equilibrium? Would there be more or less alkyl bromide product present at equilibrium? . Two dehydrations can occur on glycerol, the principle carrier molecule in vaping devices....
1. The reaction web includes most of the reactions of enolates we have studied. The products of these reactions can be treated with other reagents to generate new functionality - think synthesis! Make up your own examples - e.g. What if you treated compound D with CH,MgBr? In the table, summarize the types of products produced from these reactions. CH3 MgBr acid quench acid quench NaOH, H2O EIO OEt acid quench acid quench acid quench D LIAIHA acid quench acid...
The conversion of methane into products that contain two or more carbon atom, such as ethane, C2H2, is a very important industrial chemical process. In principle, methane can be converted directly into ethane and hydrogen. (1) 2CH4(g) C2H6(g) + H2(g) In practice, however, this reaction is carried out in the presence of oxygen: (2) 2CH4(g) + 1/2 O2(g) C2H6(g) + H2O(g) a) Using the thermodynamic data at 298K, determine ΔG° for each reaction. ΔGf° (kJ/mol) ΔGf° (kJ/mol) CH4(g) H2(g) 0...
Question 30 (2 points) What are the expected major products of the reaction sequence shown below? 1. 03 2. H20 e OH O=C=0 OH II III IV V O a) I and IV Ob) II, III and IV Oc) I and II O d) 1, III and IV Question 31 (2 points) A compound with a molecular formula of C10H1202 has the following 'H NMR spectrum. Which of the following structures is consistent with this spectrum? 2 o OCH2CH2CH3 0...
QUESTION 1 Any reaction involving a carbonyl group and a strong acid begins with the same first step, which is __________________ of the carbonyl oxygen. QUESTION 2 Using condensed molecular formulas (C#H#X#Y#) for your answers, predict the products of the reactions of C6H5CH2CHO (phenylacetaldehyde) with these reagents, and identify the functional group produced in the product. Note that the Tx symbol above allows you to do a subscript. a. NaBH4 / CH3OH b. 1. CH3MgBr; 2. H2O c. Ph3P=CHCH3 d....