SN 2: Mechanism: Br NaOH E2: Mechanism: Br NaOH 20 30 Methyl 1° Strong Weak 30 Preferred Alkyl Halides: Preferred Nucleophiles: Product Stereochemistry: Methyl 1° Strong 2° Weak Preferred Alkyl Halides: Preferred Base: Reagent Stereochemistry: Product Regiochemistry: Sw1: Mechanism: ~ Br H2O E1: Mechanism: Br H2O Preferred Alkyl Halides: Methyl 1° 30 20 Preferred Alkyl Halides: Preferred Nucleophiles: Product Stereochemistry: Methyl 1° Strong 20 Weak Weak Strong Preferred Base: Product Regiochemistry:
identify the mechanism this reaction is going though and write mechanism. H D Br NaOH CH COCH
with mechanism please! H Ph NaOH HO mCPBA Oz. DMS Br 09 Br
what is the mechanism?? st likely product of the following reaction? Br: NaOH roduct of the following reaction? 1.Divian vylborane 2, NaOI
Can you explain the mechanism? CH3 Br, NaOH PhCH,-CH-CH,-C-NH,
major products of reaction pleaseeee Br 1) 3 equivs NaNH2 Br 2) 1M H2SO4 (aq) NaOH ОН PC13 NaOH ЕТОН reflux LDA MeCN NH2
H3C Нас H3C CO2H Br 1. NaOH, H20 2 HJo Write a detailed mechanism for the Favorski rearrangement (shown above) which proceeds in two steps followed by a proton transfer. Then draw curved arrows that depict electron reorganization for the mechanism step below Arrow-pushing Instructions IIn OOH H3C H3C Br. :O-H
How to solve these problems - 1 c) Sony (2) HANI NH2 one has a stronger basic? c/) and is compare to R-NH2 which Resmant structural formula NaCN, DNO, 2 (i) (CH₂ CH₂ CH₂ BY unor PliAlta, Eto - Note, CH CHOM tints a conta Bra Noort, Hoy? Mk DME lip Cats Chache Br
-NH2 PCC, CH2Cl2 NaBH CN OH 8 Br 1. 3 equiv. 12 4 equiv. NaOH 1. LiAlH4 2. H2O 2. H30* 9 10 2 equiv. (CH3)2NH 1. LiAIH 2. H20 11 12 H2O 1. CH,MgCI 2. H30 13 14
Show the mechanism below for the reaction. figure out if its a sn1, sn2, e1 or e2 reaction in the process. Br NAOH