If you have any doubt then mention in the
commant.
What is the most likely first step of this reaction's mechanism? CH3 CH3CH2OH Br Сн, Br...
CH3 . . H I CoHs + KOH CH3CH2OH Сң,Сн, хүн heat Br CHCCH,CHE + dilute Na*CN + CH3CH2OH CH3 он- ..C-Br Agt Ha но For each of the following reactions, predict the major product(s), showing proper stereochemistry where appropriate. Write N.R. if no reaction occurs. Identify the type of substrate (1º, 2º, 3º, allylic, benzylic, aryl, vinyl) and give the type of mechanism by which each product is formed (Sni, Sy2, E, E). Assume the reaction is at room...
For the reaction shown below, what is the most likely
intermediate after the first step?
Question 8 5 pts For the reaction shown below, what is the most likely intermediate after the first step? BE Product NaOH Оо он сн. CH, 7
Which is the most stable Newman projection of the molecule below, assuming a Br-CH3 gauche interaction is 0.5 kcal/mol and a CH3-CH3 gauche interaction is 1.0 kcal/mol? Br CH3 - CH- -CH 2 -CH3 CH3 CH3 CH3 H Н. Br Br H H H Br H H H CH3 Br сн. сн., H a. сн. c. H d. CH Oooooooo Moving to another question will save this response MacBook AS ese
Which product is most likely for the following reaction? A, B, C, or D? кон CH3CH2OH он OCH CH3 ICH CHS си Но
2) Order the following alkenes from most stable to least stable Нас Нас с-сн, н,с Hас +C- Нас н CHs -CH3 H Hе most stable least stable (a) I (b) I (c) I ll (d) 7) Order the following C-H bonds from strongest to weakest. strongest weakest (a) (b) (c) II (d) 8) Which of the following is represents the lowest energy transition state for the addition of BH, to 2-methyl-1-propene? quCH «сHs нСи Нас (b) (a) Нив--н H H...
Draw the arrows for the 7-step mechanism for hydrolysis of an acetal to a carbonyl. Мар - + CH,CH,OH ACETAL HEMIACETAL 3 Ere X Step Step :0 OH2 H One Two H H H 16 Step 3. Step Step H H H -H Five :0: H Four H H1 Hi H → Step 6 ht H o: Step Draw the arrows for the 7-step mechanism in formation of the mixed acetal shown. Map from СН,ОН OH ܠܢ + HO H...
?
What is the IUPAC name for the compound? Н,С— СН,—CH—CH, ОН CH3 IUPAC name:
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....
No No What is the most likely mechanism for the reaction below? (HỤC HC-N-CH(CH4)2 Oswa Os o sul What is the most likely mechanism for the reaction below? Br (H3C)HC-N-CH(CH3)2 O SN²
() 1. Which of the following alkyl holides would you expect to be most reactive in a unimolecular reaction? CH3 a) CsM , CH, CH, CH, Br b) CEHCH CH BY c) CH, CCH, Br d) CH, CH2 CH CHE сн. он сня Br e) CHICCHE CH3 (4). 2. What would you expect to be the chief organic product(s) when tert-butyl bromide reacts with sodium acetylide, i.e.. CH + - CH3-C-Br + Na CECH ? CH a) 1 b) II...