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![V. How can you explain the fact that trans-1-bromo-2-methylcyclohexane yields the non-Zaitsev
elimination product 3-methylcyclohexene on treatment with base?
CH3
CH3
кон
Br
trans-1-Bromo-2-methylcyclohexane
3-Methylcyclohexene](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F5bdd1e13-ff3c-4e28-ab7c-41506e6ba8f3%2F1bf0a640-31a1-4769-ac9c-22e27688b7ef%2F1hkjnx_processed.jpeg&w=3840&q=75)
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- Elimination reactions of cis-and trans-1-bromo-2-methylcyclohexanes with NaOEt in E1OH can give the same or different main product, 1-methylcyclohexene (1) or 3-methylcyclohexene (2). Which of (a)-(d) indicates the main products? Br Br NaOEt NaOEt ELOH ELOH Me `Me Me Me cis 1 2 trans A. 1 both from the cis and trans substrate B. 2 both from the cis and trans substrates C. 1 from the cis and 2 from the trans substrate D. 2 from the cis and 1 from the trans substrateProvide an appropriate name for the following compound. 3-fluro u-methyl 5-chloro 7 OH CI F 5-chbro-3 fluro-4 methyl non-2-enol 2) Draw the molecule that corresponds to (3R,5R,6R)-5-cyclopropyl-6-ethyl-3-iodo-1-methylcyclohex-1-ene.Elimination occurs when (Z)-3-bromohex-3-ene is treated with NaNH2. Under the same conditions, 1-bromocyclohexeneundergoes elimination much more sluggishly. Explain why
- 1-Chloro-4-isopropylcyclohexane exists as two stereoisomers: one cis and one trans. Treatment of either isomer with sodium ethoxide in ethanol gives 4-isopropylcyclohexene by an E2 reaction. CH,CH,O Na* CI CH,CH,OH 1-Chloro-4- 4-Isopropylcyclohexene isopropylcyclohexane The cis isomer undergoes E2 reaction several orders of magnitude faster than the trans isomer. How do you account for this experimental observation?JF-M05 What is the product of the following reaction? H;C-CH2-CH=CH2 HBr + JF-MO5 H,C-CH-CH,-CH3 Br JF-MO5а H3C-CH2-CH2-CH2 Br JF-MO56 H3C-CH2-CH-CH2 Br Br JF-MO5c H3C-CH-CH-CH3 Br Br JF-M05dnent/takeCovalentActivity.do?16cal assigi [Review Topics] [References] Use the References to access important values if needed for this question. Draw a structural formula for the major organic anion formed when 2- ethylbutanal is reacted with Tollens' reagent. You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • If no reaction occurs, draw the organic starting material. P. opy aste CH4 ChemDoodle Previous Nex
- Which of the following is a ketone? А. (CH3)2Cнон В. СнзсоснЗ О с. снзсно D. CH3CH20CH3 What is the IUPAC nar e for the following structure? HO, a) cyclohexenol b) 3-cyclohexen-1-ol c) 1-cyclohexen-4-ol d) 4-cyclohexenol a How many Kekule structures are possible for naphthalene? A. 3 В. 4 С. 5 O D. 6Name the following compound oooo F None of these I -H (1R,2S)-2-fluoro-1-methylcyclopentane-1-carbaldehyde (1R,2R)-2-fluoro-1-methylcyclopentane-1-carbaldehyde (1S,2R)-2-fluoro-1-methylcyclopentane-1-carbaldehyde (1S,2S)-2-fluoro-1-methylcyclopentane-1-carbaldehydeexplain why cis-2-chloro-1-cyclohexanol yields a cyclohexanone but the trans isomer yields cyclohexene oxide
- how can you explain the fact that trans-1-Bromo-2-methylcyclohexane yields the non-Zaitsev elimination product 3-methylcyclohexane on treatment with baseWhat is the expected major product of reacting cyclohexane carbaldehyde jwith CH3NH2?For each reaction, decide whether substitution or elimination (or both) is possible, andpredict the products you expect. Label the major products. chlorocyclohexane + NaOCH3 in CH3OH
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