i think the answer is E, buy can someone verify? 2. Which elimination products would be...
i think the answer is D, but can someone please verify?
4. What is the major product of the following (E2] elimination reaction? Remember trans-diaxial. (d) (b) and (c) are equally favored
13. What is (are) the elimination product(s) of the following reaction Br メ A) Only I B) Only II C) Only III D) II and III Which of the following represents the rate law for an E2 reaction? A) Rate k[alkyl halide] B) Rate k[alkyl halide][base] C) Rate k[alkyl halide]2 D) Rate k[base] 14. 15. Which of the following statements about the mechanism of an E2 reaction is true? A) B) C) D) All bonds are broken and formed in...
How many alkene products can be formed when the alkyl iodide
shown below undergoes E1 elimination?
9. How many alkene products can be formed when the alkyl iodide shown below undergoes El elimination? CH3 CH CH A) 1 B) 2 C) 3 D) 4 E) 5
Can someone explain the answer too ? Thanks
Which acid-base reaction would not take place as written? Which base would not effectively deprotonate acetylene? a) i-PrMgBr b) KH c) (CH,0),CHI-i d) (i-Pr) NLi e) t-BuOK
The following alkyl bromide can give several elimination products Br Base Me Me (a) Give the expected elimination products (b) For each product, show how selective deuteration could reduce its yield relative to the other E2 products (i.e., show one deuterated derivative for each expected product)
can someone please explain how to do this with as much detail
as possible. someone tried to explain it earlier in relation to
(a,e) and (e,a) but im not sure even what that means
Bccurance of Methyl shift o. The following two elimination reactions are found to have very different rates of reaction. The cis compound produces two products and it reacts much faster than the trans isomer, which produces only one product. Explain these observations (the erence in rate...
can someone help please? mainly number 2
1) (15 points) Which of the following will give a polymer when condensed with adipic acid: (a) ethanol, (b) ethylene glycol, (c) glycerol, (d) aniline, or (e) ethylenediamine? Draw structures of all polymers formed. 2) (10 points) What is the first product formed when a molecule of sebacoyl chloride reacts with a molecule of ethylene glycol? What is the next product formed?
i did seprate questions for these 4 and i was given wrong
solutions. can you help with these
Rank the alkyl halides in each group in order of increasing E2 reactivity a. ш -сн, 2 Rank the alkyl halides in each group of problem one in order of increasing El reactivity 3. Which elimination reaction in each pair is faster? (I or II) a. сн, нс. "он II b. OH он (CH),CCI L (CHса IL но DMSO What alkenes are...
1) Consider the free radical monochlorination of 3-methylpentane and answer the following: a) How many products (including stereoisomers) are formed? _______ b) How many are chiral? ________ c) Would the major product of free radical bromination possess a chiral carbon? Yes or No 2) Which of the following functional groups can be generated in one step via SN2 or SN1 reaction? (Enter all that apply) a) Aldehyde b) Alcohol c) Alkene d) Alkyne e) Amine f) Carboxylic Acid g) Ester...
can you check that and i need help with 4
labeling the major minor products, and chrck my mistakes if
any
What alkenes are formed from each alkyl halide by an E2 reaction? Make sure to include all possible stereoisomers. Label the major product predicted by Zaitsev rule. Label the major product predicted by Hoffman rule. Label the major product that would be formed with the specified strong base. + OC(CH3)2 + OH Ulgan Chemistry I Home Work Chapter 8...