Alkyne reaction with na/nh3 they given product is trans alkene then it is reaction with br2 they given product is meso dibromo product
Extra Bonus. 7. * 1) Na, NH4). 2) B2. A. (R)-3-bromohexane D. (+)-3,4-dibromohexane B. (S)-3-bromohexane E....
a) b) What is the final major product expected for the following reaction sequence? 1) H2, Ni2B (P-2)2) C2 CCI4 meso-3,4-dichlorohexane ()-3,4-dichlorohexane (R)-3-chlorohexane 2,3-dichloro-3-hexene (S)-3-chlorohexane o 0 What is the final major product expected for the following reaction sequence? 1) Na, NH3() 2) Br2 CCl meso-3,4-dibromohexane 2,3-dibromo-3-hexene (t)-3,4-dibromohexane (S)-3-bromohexane (R)-3-bromohexane
4. Provide resonance structure(s) for the following 5. Draw structure for: a) (2,3E)-3,4-dibromo-1-chloro-1,3-pentadiene b) E-3-bromo-2-hexene 27 Dashboard Calendar To Do Notifications Inbox
QUESTION 1 Hydrogenation of 3-hexyne with Pd catalyst gives: O a. hexane b.(E)-3-hexene OC. (Z)-3-hexene d. 3-hexanol QUESTION 2 Reaction of ethanol with metallic Na belongs to: a. acid-base reactions b. Sn2 reactions c. E1 reactions O d. redox reactions QUESTION 3 If 1-hexyne is subjected first to Lindlar's catalyst and hydrogen, and then the formed product is treated with HBr in the presence of radicals, the ultimate product is: a. 1-bromohexene b.2-bromohexane c. dodecane d. 1-bromohexane
CH3 Нас CH3 CHE Pu CH3 H₂C. CH3 CH3 3,4-dimethyl-3-hexene 3,4-dimethylhexane dimethyldiethyl-1-butene 1.2-dimethyl-3-hexene 3-methyl-4-methyl-3-hexene 1.2-dimethyl-1-hexene 2,3-diethyl-2-butene Question 2 MACRO AIR Da
3) Show how hex-1-yne might be converted to: a. 1-bromohex-1-ene b. 1,1,2,2-tetrabromohexane C. 2-bromohex-1-ene d. 2-bromohexane e. 2,2-dibromohexane 4) For each compound, give the product(s) expected from (1) HgSo./H2SO4-catalyzed hydration and (2) hydroboration-oxidation. a. hex-1-yne b. hex-2-yne c. hex-3-yne d. cyclodecyne 5) Predict the product(s) you would expect from treatment of each compound with (1) dilute, neutral KMnO, and (2) warm, basic KMnO, then dilute acid. a. hex-1-yne b. hex-2-yne c. hex-3-yne d. 2-methylhex-3-yne e. But-1-ene → butan-2-ol 6) Show...
19. What would be a correct rate law for the following reaction? cI +CEN Na a. reaction rate-K[A]o[B] b. reaction rate xAl'[B] c. reaction rate = K[A]: [8]。 d. reaction rate K[A] [B]2 e. reaction rate: K[A]2[B]1 f. none of a-e 20. What is the major product formed upon treatment of (R)-2-bromohexane with sodium cyanide? a. (R)-2-cyanohexane b. 1-hexene c. 2-hexene d. (S)-hexanol e. (S)-2-cyanohexane f. none of a-e
solution of question d (4 points) Consider the basis of R5 given by with b2 (2,-1,-5,-4,7), b3-(3, 2,-7,-5,9) b4 2,1,4,4,-5) bs (-1,0,1,2,0) The MATLAB code to produce the basis vectors is given by b1 11,0-2-2.3], b2 -12-1.-5-4,7T, b3 13-2-7-5,91, b4 [-2,14.4-5T, b5 1-1,0,1,20 Let S denote the standard basis for R a Find the transition matrix P P,s PB,s b. Use the previous answer to calculate the coordinate matrix of the vector z ( 1,5, 4, 3, 3) with respect...
If you did an SN2 reaction with R-2-bromobutane what would the stereochemistry of the product be? a) R b) S c) achiral d) racemic mixture e) NA If you did an SN1 reaction with S-3-bromohexane what would the stereochemistry of the product be a) R b) S c) achiral d) racemic mixture e) NA
(1,3), с %3D (2,1), d (3,4) (1,2), b (4,2), f (5,3) and (5,5). Let 5. Let a = е 3 - {a, b, c, d, e, f, g} be the set of these 7 points. We define the following partial order on S: We have (r, y)(', y) iff x< x and y < / Draw the Hasse diagram of S S 6. We consider the same partial order as in Problem 5, but it is now defined on R2....
IZDI 4) What is the major organic product of the following reaction? NaOCH_CH: A) 2,3-dimethyl-2-hexene B) (E)-2,3-dimethyl-3-hexene C) (2)-2,3-dimethyl-3-hexene D) 2-isopropyl-1-pentene E) 2,3-dimethyl-1-hexene ila nf the following statements correctly describe(s) E1 reactions of