Can another check if these are right ? 9. 3-methyl-2-heptanolH,So. CAI 10. 3-methyloctanalNaBHs eth CI Cr...
1 H NMR 2-METHYL 2- PENTANOL Peak Chemical Shift (δ) Multiplicity† H‡ Peak Chemical Shift (δ) Multiplicity† H‡ 1 7 2 8 3 9 4 10 5 11 6 12 Specify the multiplicity as a singlet (s), doublet (d), triplet (t), quartet (q), or multiplet (m). Specify the number of hydrogens associated with each peak. THE TOPIC IS RELATED TO H-NMR AND THE GRAPH IS RELATED TO THAT ALSO. THE GRAPH SHOWN ABOVE IS FOR 2-methyl 2-pentanol ....
Leto 1. 2-methyl-1-butene memome IUPAC Nomenclature Practice 2. 2-methyl-3-heptyne 3. (z)-3-ethyl-4-methyl-2-hexene Iy-01 001 9pocz o00'1- 4. 2-propохурепtane ent & Uni S. 4-methylhexanoic acid P7 wnuuny Jod 0. (E)-2,3-dichloro-4-ethyl -2 -hexene 7. 3-ethyl-2,3-dimethyl -2 - pentanol etration Pov racterized lecay (phor 8. 5-chloro-4-methyl-3 -heptanone ) eaap decay (ene Fission Fusion 9. 3-phenyl-1-propyne dioac Туре HI t Trans 10.2-methylcyclopentanol 11. (Z)-3-methoxy-2-pentene 12.3-bromobutanoic acid
Match each reaction with its reagents. HO CI N 1 + enantiomer -OH 4 3 + enantiomer + enantiomer 6 5 OH w 8 } OH Hol Bre 10 Br + enantiomer to C 10 Br + enantiomer Br 11 Br 12 Reagents: B.) NBS, hv A.) PBr3 C.) - D.) NaOH E.) NaNH2 F.) Br2 H.) Cl2, H2O G.) HCI 1.) HBO J.) H2 (1 eq), Pt K.) Na, NH3 L.) H2SO4, H2O 0.) M.)1. Hg(OAC)2 2. NaBH4 N.)...
for f - j draw structures pls help with #1 as well f) 4-methyl-2-pentene 9) trans-8-ethyl-3-undecen h) E-5-bromo-4-chloro-7,7-dimethyl-4-undecene i) Z-1,2-difluoro-cyclohexene i) 4-ethenylcyclohexano Predict the major organic product or products of each of the following reactions. a) (CH3),CHCH-CH: H2SO4 HO b) (CH3),CHCH-CH, 1. Hg(OAc), H20 2. NaBH4 1. BH-THF c) (CH3),CHCH-CH2 2. H,O, NaOH
MUNITY COLLEGE ABNO, 6. Ba(NO) AgNO HNO, 7. 3 (a) H,SO NH,Ci 8. 4 (ag) (a) H,SO U) NaOH (aq) 9. H.SO Na,CO, 10. 4 (aqh H.SO Na,PO 11 4 (aq) + Ba(NO,) H.SO4() 2 (a) 12 13. H,SO +HNO,a) 4 (aq)
V Arrangw the followong molecules so that reactivity with KSCH3 in dimethylsulfoxide increases from left to right VI. complete the following reactionssupplying the missing reactants. reagents, or products... VII. oxane cane be made from the reaction of 5-bromo-1-pentanol VIII. show a atepwise sequence for each of the following transformations HI PLEASE HELP, ive been struggling with prgo and this is our exam review if you could help and/or give explanations it would really help. THANK YOU! V. (10 pts) Arrange...
1.The main product of the reaction between p-cresol and Br2 / FeBr3 is: 3-Bromo-4-methyl phenol 2-Bromo-4-methyl phenol 2-methyl-4-bromine phenol 3-methyl-4-bromine phenol 2.Which of the following compounds is the least reactive in the nucleophilic substitution with NaOH? 2,4-dinitrochlorobenzene m-nitrochlorobenzene o-nitrochlorobenzene 3,5-dinitrochlorobenzene 3.What is the mechanism (s) for the reaction of 4-bromo-1-nitrobenzene with sodium hydroxide to form 4-nitrophenol? bimolecular nucleophilic substitution (Sn2) aromatic nucleophilic substitution by addition-elimination aromatic nucleophilic substitution by elimination-addition aromatic electrophilic substitution 4.which of the following is the correct...
Balancing Equations Balance the following chemical equations. Sicla(l)+ SiO (s)HCl(aq) 2. As 3 NaOH NaOH H2 3. Ha Au + н,s но-> voC+ H20 5. -Hg(OH)2 + H3PO4 H20 SiO2 + HF→ SiF4 + -ho 7. 2 Zn Ha → ZnClz + H2 8. HCIO4 02(g)HO HNOs(aq) NH4NO3 ut Chemistry http://chemistry.about.com Balancing Equations Balance the following chemical equations но 2. cr→ Naa 3.4 A1 +302 -Al2O3 NH3 5. CO(g) + HO 6. FeO3(s) +-- CO(g) → Fel)+ CO2(9) 7. HSO_...
please help me with questions from 3-10! and the bonus. thank you so much Directions: Place your answers to the following questions in the provided spaces. (12 PTS) 1. What is the hybridization of the carbon atoms numbered 1 and 2 respectively in the following structure? -CU CECH A. B sp,sp? sp, sp sp, sp sp', sp sp, sp Ans. 2. What is the IUPAC name for the molecule shown below? os B. C. D. E. (E)-5-methyl-5-hepten-1-yne (2)-5-methyl-5-hepten-1-yne (E)-3-methyl-2-hepten-6-yne (2)-3-methyl-2-hepten-6-yne...
6. Consider the sum of the first 10 numbers: 1+2+3+4+5+6+7+8+9+10. Can you change some of the plus signs to minus signs so that the resulting sum is 0? For example: 1+2-3-4-5-6+7-8+9+10=3. This is close, but not 0. Provide a solution or show that there isn't one.