Place the following carbocations in descending order of stability. Explain your answer. A CH3 B CH C CH CH Give detailed Solution with explanation needed. don't give Handwritten answer.
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- Rank the following compounds in order from most able to leave stable, explain your ranking. Use image as referencePredict the major products of the following reaction. Be sure to use wedge and dash bonds to show the stereochemistry of the products when it's important, for example to distinguish between two different major products...predict the major and minor productand explane it
- What is the Iupac name answers of all those questions from (d) till (h)???Select the keyword or phrase that will best complete each sentence. Key terms: backside carbocation elimination frontside hyperconjugation inversion maintenance nucleophile product racemization stronger substitution weaker Alkyl halides undergo A orbital. reactions with Brønsted-Lowry bases. is a sp² hybridized and trigonal planar and contains a vacant p All SN2 reactions proceed with in attack of the nucleophile, resulting of configuration at a stereognic center. Spreading out charge by the overlap of an empty p orbital with an adjacent o bond is called Equilibrium favors the products of nucleophilic substitution when the leaving group is a base than the nucleophile. According the to Hammond postulate, the stability of the determines the rate of its formation. The formation of equal amounts of two enantiomeric products from a single starting material is called A is an electron-rich compound, which donates a pair of electrons to an electron deficient compound, forming a covalent bond.…c) Rank the following compounds in order of increasing reactivity toward nucleophiles. Explain your reasoning briefly with reference to structural features. or wy CI A
- Rank the following carbocations in order of increasing stability.Provide to llaving Br a detailed, step by step mechanism for the reaction OCH₂CH3₂ OCH₂CH3 OCH₂ CH3Predict the product of the reaction shown below. a) b) Br2, FeBr3 Br c) Give detailed Solution..don't ? give Handwritten answer d) Br -Br Br
- Use the References to access important values if needed for this question. Draw the structure of the product that is expected when the following compound is treated with concentrated H2SO4. он H2S04 ? heat CH3 You do not have to consider stereochemistry. • In cases where there is more than one answer, just draw one. ited opy Bste [F CH4 ChemDoodle Retry Entire Group 3 more group attempts remaining Submit Answer Previous Next Email Instructor Save and Exit Cengage Learning | Cengage Technical SupportSynthesis - Drawing Saved Synthesize the following compound from cyclohexanol, ethanol, and any other needed reagents. он Part 1 out of 2 plnts Preparation of organometallic reagent: еВook Print References A B CH3CH2OH CH3 CH2MGB. draw structure ... Draw the intermediate product above and select the correct reagent for A. O Br, O NaBr O HBr O Select the correct reagent for B. O Mg O MgBr2 O MgI, O MgO Hin Soluti raw 11 e here to searchFor the following compound: ته HO Draw a mechanism for the tautomerization process under BASIC conditions: Mechanism A: H-5: ·H Mechanism B: H-5: -H Mechanism C: H-0: H-O: Mechanism D: . © H-OH2 ل سے -H م - H-O: H-OO که فری -H H-00 H... H ·H H H m-o-m H: H H H H... H ته + H-OO H-00 O. H :: H © H-O-H -H