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- What is the mechanism of this reaction? Plz do Asap...!Profiles Tab Window Help ALEKS - Tiffany Te-L-Peng - L X = sl.exe/10_u-IgNslkr7j8P3jH-liGBdp5ulp5VqUnMDyPOVaX6q0CRPLZSQ5NeEtFRBekLt6yRz O SUBSTITUTION REACTIONS Identifying resonance stabilized carbocation intermediates in... Substrate For each of the substrates below, identify whether: (A) the rate of substitution doesn't depend on nucleophile concentration and (B) the product distribution from substitution gives a 50/50 mix of enantiomers. If you answered "yes" for the first susbtrate, draw the intermediate that forms during a nucleophilic substitution reaction in the space below the table. 'Br á Br Are both A and true? Oyes Ono + Oyes O no Oyes Ono Oyes Ono ㅂ Click and drag to start drawing a structure. X C с X TiffaA student runs the reaction shown here and obtains the 'H NMR spectrum shown. Determine the product of the reaction and draw the complete, detailed mechanism of the reaction. 1. excess CHI 3.4 3.3 ? ? NH2 2. Ag20 3. Д 10 9 8 7 6 3 2 1 Chemical shift (ppm)
- e Edit View History Bookmarks Profiles Tab Window Help с ALEKS ← O SUBSTITUTION REACTIONS Understanding how the degree of substrate substitution... Br www-awu.aleks.com/alekscgi/x/Isl.exe/1o_u-IgNslkr7j8P3jH-liGBdp5ulp5VqUnMDyPOVaX6q0CRPLZSQ5Neibwylv0Xa9PGXX794jCYYPc4Wwmj2... Explanation A 2 X A ALEKS - Tiffany Te-L-Peng - L X + Substrate + Bri Br r Use the first column to rank each substrate by the rate at which it will undergo SN2 ubstitution. Use the second column to rank each substrate by the rate at which it will undergo S1 substitution. 3 Check с 54 $ Rate of S2 (Choose one) ▼ (Choose one) ▼ (Choose one) ▼ % Rate of S1 5 (Choose one) ▼ (Choose one) ▼ (Choose one) ▼ G Search or type URL B A 6 MacBook Pro X & 7 3 ☆ * 00 8 US ODDOD 0/5 © 2022 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center + O $ 61 9 432 e ) O Q I' a 90 Tiffany V ? L de Ar AccessibilityShow the mechanism of the ff. reaction. Show stereoisomers if possible.the reaction below, select all the atoms in the leaving group and identify the elementary mechanistic step. See Periodic Table see Hin Part 1 H.C H.C. CH CH,
- Predict the products of each reaction. If the product has stereochemistry, draw the products using dash wedge notation. Draw all stereoisomers formed and indicate if the product is achiral or chiral. Draw a mechanism for each reaction clearly showing how the product stereochemistry is produced. You are not required to draw the final step(s) in the mechanism for reactions involving organometallic intermediates.Pls help ASAP. Pls do all asked questions. Pls identify the reaction below.Using drop down answer the questions which correctly characterizes the mechanism of the reaction shown? CH3SNA, CH3OH SCH3 Br # of Transition States? = choose your answer... # of Intermediates? = choose your answer... Rate Determining Step?= choose your answer...
- Does the following SNAr reaction occur accordingto an addition-elimination or an elimination-addition mechanism? Motivate.Don't provied handwriting solution. 0Can you please explain the reasonin behind why we split the molecule the way we do to obtain the desired product in addition to showing the mechanism? Thank you!Answer fast i will give upvote Write down the identification reactions for lodine. Specify the reaction conditions.