can someone please explain how to do this with as much detail as possible. someone tried...
Please explain how to draw the newman projection as well. 2. Explain why the following compound reacts to give a mixture of alkene stereoisomers in which only the cis-dimethyl isomer contains deuterium. Hint: draw the alkyl halide in a Newman projection. You will be asked to do this on midterm 1. Br CH,CH,OH Das * Change CACHON le CH3 C'H + CH3CH,0. H;c Stvong base
organic chemistry answer is D. Can someone please explain why? 3. Which reaction would proceed the fastest? (A) CH3CH2OCH2 + OH → CH3CH2OH + COCH3 (B) CH2CH2SCHz + OH → CH3CH2OH + SCH; (C) CH3CH2N(CH3)2 + OH -- CH3CH2OH + "N(CH3)2 (D) O CH3CH2OSC6H.CH3 + OH - © CHỊCH,OH + OSCH,CH
3 & 4 please Draw all possible El elimination products and indicate which alkene is the major product: CH3OH CH3 a) HC-C-ci CH3 CH3CH2OH CH3C430H CH3CH2OH Br CH3CH2OH I X ORSOGON CH3OH Br brow all possible E2 elimination products and indicate which okene is the major product CH, ON CH, OH CHÚCHONa CH,CH OH CHÚCH ONa CH,CH, OH CH3CH2ONa d YoX CH₂CH₂OH CH,CH OH (CH3),COH TONE CH,(CH)CH,OH CHCH,ONa CH,CH,OH CH,CH, CH,CH,ONa CH,CH, OH CH,
Critical Thinking Questions -SHOW your work or Explain how you found the answer. 1. Write the substitution reaction for one NH, replacing one H:O in [Cu(H:O)%]. Assume it uses a dissociative mechanism. 2. Then, write it again, but use 3-D drawings, to show the structures of the reactant complex, its intermediate, and the product. A template for octahedral geometry has been given, but you will need to make a complete drawing for the geometry of the intermediate state. 3. For...
please explain in as much detail as possible so I can understand 2/4 6. Identify the major and minor products for each of the following reactions, considering the base that is used: NaOH (CH3),COK b X CH)COS , ) NaOCH CH; (CH3),COK
how do i know which Hydrogens i affect? what do i do here? can someone explain what im supposed to be looking for with drawings too? i thought this was an aldol condensation but this says its a michael reaction and the answer is C. thank you so much! 290. Predict the product: CH2=CH-C + OH CH=CH-C°. CH-&-CH2-8-CzHs Hot H2O H O=0 -C-C-C2H5 о но No reaction: base is too weak to allow deprontonation. CH2 e) C2H5-C-C-C-C2H5 CH2 HG он...
can someone show me how to do the work and explain it to me 10. What is the leaving group in the following reaction? CH,CHOH + HCI , CHCHCI + 0 А. ОН НО CH3CH, CI D.
Can someone explain to me how to solve these. I dont understand how these answers are correct. II. (16/100) Which structures represent likely products of the following reactions? Circle the letters corresponding to the structures of your choice. Each wrong answer will receive negative points. NC - ایک عام سا محلاه بعد - پوس-HC | ء Br , H2O H3CH2COH-3-2 methylene H CH H- CH, HgCCHCH CECHCH HgCHCCH CH3
can someone show me how to do the work and explain it to me TIEM210-W03, Fall 2019 Prof. J. Fiorito 13. What is the rate limiting step in the following reaction? (CH3)3CCI + H2O - (CH);COH + HCI A) (CH3)3CCI -- (CH3)3C' + cr B) (CH3)3C + H2O - C) (CH3),C-OH + H20 - D) H0+ + cr H (CH3)3C-OH, (CH3),COH + H30 Cl + H20
Can someone explain why the answer is not cis-1,2-cyclohexanediol and ethanol? Question 7 What are the products of the reaction shown below? O CH heat O IH OA. cyclohexanone and ethanol O B. cis-1,2-cyclohexanediol and ethanol O C. trans-1,2-cyclohexanediol and ethanol O D. cyclohexanone and ethanal 0 E. cis-1,2-cyclohexanediol and ethanal