In chair cyclohexane a large group have a strong preference for the equatorial position. This is due to the Ogauche effect anti interactions hyperconjugation 1,3-diaxial interactions
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- Please help with 4c, 4d, and 4e. We havent learned kaw of equivalents so please do 4c a different way. thank youPradet te major produet for he folewing trenatormation, e miedu of siereechamistry, when spplie Me. 1. ВНз THE 2. NaOH H2O2 H2O OA Oc OD. Me. OR HO Me OH Me- OH OH MeProvide the most stable chair confirmation of cis-1-tert-butyl-4-methylcyclohexane
- Find and select tio conformers of the same trisobstituted cyclohesane derivative from the brary of molecules drawn below CH3 OH CI OH CH3 HO CH3 но HO. CH3 но CH3Rank the following groups in order of priority from highest (1) to lowest (3). < < -COO- -CH3 -NHCH3ll 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) Butylamine
- В. Draw the structure: - 2- methyl -1, 4- cyclohaxadiene |- isopropyl cyclohexadi ene 1,3, S- cyclo haptetriene ·2-methyl-1,4- 2. 3. 4. 4- 150propyl-2- methyl- 1,3- penta di ene 5. 2- e thyl-I,4-di methyl eyclopentane dimethy) eyclopentaneHow many kinds of chemically non-equivalent hydrogens are there in each of the following compounds? a b a CH₂ CH-CH₂ b b CI-CH₂- xeview Toples] [References] How many kinds of chemically non-equivalent hydrogens are there in each of the following compounds? Phenobarbital Orangulizer) The number of chemically non-equivalent hydrogens is The number of chemically non-equivalent hydrogens is How many kinds of chemically non-equivalent hydrogens are there in each of the following compounds? CH₂-CH-CH-CH₂ CH₂ CH₂-CH-CH-CH₂ The number of chemically non-equivalent hydrogens is ob bon Submit Answer The number of chemically non-equivalent hydrogens is The number of chemically non-equivalent hydrogens is The number of chemically non-equivalent hydrogens is Retry Entre Group 2 more group attempts remaining- с app.101edu.co Identify which of the following compounds is meso. I H₂CO H III H C H₂CO HCI Н A) 1 B) II Question 52 of 67 C) III D) IV OCH H₂CO "CH3 H C H CH₂ OCH₂ IV Н H₂CO H.C Н OCH, "H CH3 CH3 OCH₂ S В Sub
- A B C D E 1. NaBH4 2. H3O+ 1. CH3MgBr 2. H3O+ 1. (CH3)2CuLi 2. H3O+ 1. CH3Li 2. H3O+ 1. (CH3CH2)2CuLi 2. H3O+A eFundi : Home : Overview E NCHE 121 - Module test - Versio X G Which one of the alkenes can for x b My Questions | bartleby + A https://docs.google.com/forms/d/e/1FAlpQLSeaeyD2qYYYa712LcEehfMLha7DEaTq1KXQ5g7o2byUrT8CnA/formResponse Question 4: The alkene 2-methylbut-2-ene reacts with hydrogen cyanide (HCN) to form the Markovnikov product. Write the preferred IUPAC name of the main product of this reaction. [Use lowercase letters. Do not use spaces if it is not required in the name.] * Your answer Question 5: Which statement about electrophilic addition reactions is not true? * Markovnikov's rule explains why the addition reactions of unsymmetrically substituted alkenes are regiospecific. Markovnikov's rule does not apply to internal alkynes. The larger amount of the nucleophile will bond to the more stable carbocation during an electrophilic addition reaction. None of these statements are correct. O All of these statements are correct. Question 6: The mechanism in Figure 6 produces…Q4 * 1,3-thiazolo[4,5,b]pyrdine 1,5-thiazolo[4,5,b]pyrdine 1,3-thiazol[4,5,c]pyridzine 6-thiabicyclo[4.5]decane 1-thia[5.6]decane Both are wrong Q5* ΟΟΟ Q6 * 2H-1,3-oxazete 4H-1,3-oxazete 2H-1,3-oxazane 4H-1,3-oxazane