Which of the following nucleophiles would tend to favor conjugate addition to an alpha beta unsaturated...
This reaction is an example of conjugate addition of a nucleophile to an alpha, beta-unsaturated carbonyl. Draw the two resonance structures of the enolate anion intermediate for this reaction.
Which of the following reagents do not react with ketone carbonyls? a. NaBH4 b. (CH3)2Culi c. LiAlH4 d. CH3MgCl . Treatment of an alcohol with which of the following would produce an ether? a. CISI(CH3)2(C(CH3)3) b. NaH, CICHOCH3 c. NaH, CH3CH2Br d. all of these Conjugate addition to a,B-unsaturated carbonyl compounds is characteristic of a. mild, reversible nucleophiles b. strong, irreversible nucleophiles c. wet oxidizing agents d. large weak electrophiles e. small strong electrophiles f. alkyllithiums
b. NaH, CICHZUCH3 _ 5. Conjugate addition to a, B-unsaturated carbonyl compounds is characteristic of a. mild, reversible nucleophiles b. strong, irreversible nucleophiles c. wet oxidizing agents d. large weak electrophiles e. small strong electrophiles f. alkyllithiums rcle the bond below that does not absorb above 1400 cm? d. C=0 b. C=C a. C-H e. C=N c. C-o 7. Which regent below would effectively yield a nitrile from a benzenediazonium ion a. NaCN c. NaNH. e. NHANH
The following Aldol Condensation produces a mixture of SIX -alpha, beta-unsaturated carbonyl products. DRAW the structure of all Six the alpha, beta-unsaturated products obtained.
Which of the following reagents does not add to an alpha, beta-unsaturated ketone in a1, 4 -connieaie addition? HCN (CH_3)CuLi CH_3MgBr CH_3CH_2NH_3 Which structure is the enol form of the compound at the right? Which of the compounds below will undego decarboxylation upon heating? 3 only 1 and 3 2 and 3 2, 3, and 4 Which compound cannot form a lactone?
5) Draw the Structure of ALL the alpha/beta unsaturated carbon obtained as the dehydration products from the following aldol cond ůco + nsaturated carbonyl products that would be he following aldol condensation: NaOEt 6) The Aldol Condensation below provides only ONE PRODUCT. Provide the structure of the Aldol Dehydration Product and a Full Mechanism to account for its formation. C. –
4. Provide a complete curved-arrow mechanism for each of the following transformations involving conjugate addition Note that no stereochemistry is shown or implied in any of these reactions, and you may neglect it in your mechanisms as well. a. For this mechanism, you may assume that the reagent NaBH.CN behaves just like NaBHs, and that it preferentially performs 1,4-addition to unsaturated carbonyl compounds. O ! OME OMe H 1. NaOE, ETOH 2. NaBH CN, MOH oMe ОMe OME OME EtOXOE...
Explain 5. Which of the following underlined alpha hydrogens are the most acidic? A) ping underlined alpha hydroul it muc stalde. B) Section: 17-1 Section: 17-1 E) D) CH3-CH O CH3-C-CH2-CH CH3-C-CH2-C-OCH 3 CH3-C-CH3 CH3-C-0-CH3 11.
2) Which of the following underlined alpha hydrogens are the most acidic? A) 0 CH3-CH B) CH3-C-CH2C-OCH3 C) CH3-C-CH2 CH D) CH3-C-O-CH3 E) CH3-C-CH3
Understand alpha helices and beta pleated sheets Question Which of the following statements is not true about R groups in B-pleated sheet? a. The R groups of the peptide chain point outside. b. The R groups are attached to the carbons and extend above and below the folds of the pleat. c. The amino acids tend to have smaller R groups. Select the correct answer below: a and b a and c b and c only a FEEDBACK MORE INSTRUCTION...