Rank the following alkenes in order of decreasing values of Amax- structure A structure B structure C structure D Highest Value | Structure D | Structure C | Structure A | Structure B
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- Electron pairs CH3 .. Erase H3C - С — СІ: H3C – S- CH3 CH3 CH, CH3 THF/H,0 + H,C--CH, CH C- CH CHs CH, Use curved arrows to write the first step of this nucleophilic substitution mechanism. :ö: | :ö:22:52 y & UPU .. 3 all 35% + PicsArt_02-25-08... / QA\ give 7he 1UPAC name ofthe following: CH,-CHz - c - CHe -C- CH, CH, CHE CHe CH B/ fnd The hybridization, shape and Anagle of:0 - CaH4 Q\ A\ 1- Alkenes are soluble by 2- What does The Branching do Wth The baing Pojent 3? B\ PrePare [2fen tyne] from Acetylene Q Complete The flowing reactions ... CHs-C=C-CA3 Li CHs -CEC-CH3 HI of 2 mole CH -C ECH. H.O CH3 HCID. HOw many aistinct terminal alIKynes exist with a molecular formuia of C5H8! c. How many distinct internal alkynes exist with a molecular formula of C6H10? 4. Which of the following has the lowest b.p? a. 3,3-dimethyl-1-butyne; b. 1-hexyne с. 2-heptyne; d. 3-hexyne; e. 1-decyne. 1 5. Will the reactions shown below go the direction as indicated? + CHOMaBr CH
- Each of the following line structures can be described as a bicyclononane except for... OA. O B. All of these structures can be accurately described as bicyclononanes Oc. OD. OE AMoving to another question will save this response. esc @ 2 4 5 6Ti Which of the following is the most stable carbonation? ed 50 4 1 3 O a. 1 O b. 3 О с. 2 O d. 4 US PAGE NEX cer 17: lecture (1) 4/4/ Jump to.. at @ PUelC All rights reserved TOSHIBA - | -- | - |--| - | - | B/O FS F6 F7 F9 F10 F1 24 & A 45. Cychonexene dnd KMNQ4 In 6.Onknown 2 Calkene) reactants. and KMn to OH Mr Products 7. Gyclonexene and Hz SQu H-O to 1.
- ll mobily ? 4:13 PM O 21% O < Homework - carboxylic a... CH3CHCH2CH2CHCH3 CH3CCO2H CH3 (c) .CO2H (d) CH3 CH3CCN CH3 (g) Br (h) CN BRCH2CHCH2CH2CO2H Q2: Draw structures corresponding to the following IUPAC names: (a) cis-1,2-Cyclohexanedicarboxylic acid (b) Heptanedioic acid (c) 2-Hexen-4-ynoic acid (d) 4-Ethyl-2-propyloctanoic acid (e) 2-Cyclobutenecarbonitrile Q3: How could you convert butanoic acid into the following compounds? Write each step showing the reagents needed. (a) 1-Butanol (b) 1-Bromobutane (c) 1-Butene How could you convert each of the following compounds into butanoic acid? Write each step showing all reagents. (a) 1-Butanol (b) 1-Bromobutane (c) 1-Butene How could you convert butanenitrile into the following compounds? Write each step showing the reagents needed. (a) 1-Butanol (b) Butylamine16. Which of the following is the most stable carbocation? a) *CH3 b) CH;CH,* c) (CH3),CH* d) (CH;);C*C OWLV2 | Online teaching and learning resource [Review Topics] [References] Use the References to access important values if needed for this question. Draw the structural formula of the product that would form when 1,3,4-trimethylcyclopentene undergoes catalytic hydrogenation. • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. C opy aste ChemDoodle M) Submit Answer Retry Entire Group 4 more group attempts remaining Previous Next Email Instructor Save and Exit
- OWLV2 | Online teachin X ate Univ Assignment 4_Reactions of. https://cvg.cengagenow.com/ilrn/takeAssignment/takeCovalentActivity.do?locator=assignment-t [Referenc of Alkenes and Alkynes_Chapter 8 (8.1-8.7)_Spring Draw structures for the alkene (or alkenes) that gives the following reaction product. CH3 H/Pd CH3 You do not have to consider stereochemistry. • Submit more than one structure only if the structures are constitutional isomers • Draw one structure per sketcher. Add additional sketchers using the drop-down m • Separate structures with + signs from the drop-down menu. pt 自ノラ (F e to searchWhich alkene would be the LEAST stable?\Identify the alkene that is the most stable and the alkene that is the least stable. Most stable = Explanation for most stable carbocation: 11 ; Least stable = III