Can you please tell me whether the product is cis or trans? Exercise 1. 4 2...
Can
you please tell me which one is CIS and which is trans (starting
materials)?
Exercise 290looib bixo 2i0tn 2 CN NC 6-455-2 shixo aliti CN Snoro CN 3. + 2bausgon ologib NO2 EIL NO2 NO2 5 A/
Can you show me the mechanism for 1-Butanol to Cis-2-Butene and
trans-2-butene?
(Does the carbocation shift from c1 to c2, then a hydride shift
from c2 to c1 (kicking off the water), then another water molecule
takes a hydrogen from c3, with the electrons then going from c3, to
share between c3 and c2?)
Many carbocation rearrangements involve hydride shifts (Section can also migrate to a positively charged carbon. in the direction that leads to a more stable carbocation. 5.12)...
Can
someone tell me if these structures are correct? can you please
write the correct structures as well. i am also have a bit of
trouble with questions 4-6. please help thank you.
3- Draw the structural formulas for the following compounds: a))2,2,5,5-tetramethylheptane C H3 b) 6,6,6-trichloro-1-hexyne ) 3-chloropropanal Cy Hi CO d) trans-2.2,5,5-tetramethyl-3-hexene CH c l e) 3-methyltoluene 3-bromo-5-methylphenol CaH2rO F10 F9 4- Complete the following reactions a) b) Br c) [Ol HaC он HO CH3 5- A student...
A. 1-cis, 2-cis B. 1-cis, 2=trans C. 1=trans, 2-cis D. 1: Enter Your Answer: OA OB OC OD A Correct Draw the major product of the following reaction. Question 9 Br L -CH3 we 3-chs H3C CH3 Create OscerSketch Answer 9 Not Submitted Draw the major product of the following reaction. Question 10 H3CH HO CH3 Create OscerSketch Answer 10 Not Submitted Save Answers 8 Submissions Left
Please tell me if i have part (a) correct or not?
and answer part (b) for me please with clear hand wrriten
please.
Question 8) A) Below is a reaction scheme you performed in lab to reduce 4-+-butylcyclohexanone to the corresponding cis and trans secondary alcohol isomers. In lab you used NaBH4 to reduce the ketone, but state whether it is also possible to use LiAIH4. If so, why did we choose NaBHs instead of LiAIH? OH NaBH4 MeOH 个个and...
HI. Can someone please differentiate the two NMR of cis and
trans Nepetalactone? Like where are the sp2 hybridized C-Hs and all
other aspects of NMR. I labeled all the C's and H's from the
structure but can't differentiate between cis and trans
Nepetalactone. It includes both 1H and 13C NMR. Thanks in
advance.
Cis-Nepetalactone O He 7 10 4 8 9 462626* “64626. 48 44 44 42 40.- 4双3.o 2* 24 24 22 20 ,8 16 '4 1.2 Trans-Nepetalactone...
Can you answer these please?
Aldol Assignment Write the answers to 1,3 & 5 on a sheet of paper and be prepared to email it to me. 1. Why is it important to maintain equivalent proportions of reagents in this experiment? 2. What side products do you expect in this experiment? How are they removed? 3. The geometric possibilities for products are cis/cis, trans/trans or trans/cis. Which isomer do you think is the major product and why?. 4. What evidence...
21. Which of the following are coordination isomers? (a) cis-[CoCl2(en)2]Cl and trans-[CoCl2(en)2]Cl (b) [Cr(NH3)[Fe(CN) ] and [Fe(NH3)6][Cr(CN)] (c) [CoBr(NH3)sSO4 and [CrSO4(NH3)s]Br (d) [Co(NO2)(NH3)s]Cl2 and [Cr(ONO)(NH3)s] Cl2 (e) Both (b) and (c) Review your answer (CIRCLE): Are you (1) confident; (2) somewhat confident; or (3) unsure/guessing?
21. Which of the following are coordination isomers? (a) cis-[CoCl2(en)2]Cl and trans-[CoCl2(en)2]Cl (b) [Cr(NH3)[Fe(CN) ] and [Fe(NH3)6][Cr(CN)] (c) [CoBr(NH3)sSO4 and [CrSO4(NH3)s]Br (d) [Co(NO2)(NH3)s]Cl2 and [Cr(ONO)(NH3)s] Cl2 (e) Both (b) and (c) Review your answer (CIRCLE):...
Can
you please tell me if these are ortho, meta, or para?
CN LEN
The cis-configuration of 2-butylene is higher in energy than the trans-configuration by 8.3E‑21J. You can synthesize trans-butylene with 100% yield. A customer wants to purchase your product but insists on 99.999% trans. What is the maximum temperature you can allow the product to be stored at to meet the customer’s specifications?