Name the following compounds: m-Diethylbenzene 1,3,4-trichlorobenzene 5-bromo-2-chlorophenol
1. Write the structure of trans-3-bromo-4-ethylcyclopentene. 2. How many chiral carbons are in the above structure? 3. Draw the structure of 3-chlorophenol.
Draw the structure of 4-bromo-2-hexyne.
1. Write the structure of trans-2-bromo-3-ethylcyclopentane. 2. How many chiral carbons are in the above structure? 3. Draw the structure of 3-chlorophenol.
Draw 3-bromo-2-chlorocyclohexanone in the space provided. Draw 3-bromo-2-chlorocyclohexanone in the space provided.
Draw a dash-wedge structure for the following? (a) (1R)-1-bromo-1,3,3trimethylcyclohexane (b) (2S, 4S)- 2-bromo-4-methylhexane provide r and s please
Draw the mechanism and label products and reactants for the synthesis of aniline to 4-Bromo-2-Chloroacetanilide: Aniline + Acetic Anhydride --> Acetanilide + Acetic Acid Acetanilide + Bromine --> 4-Bromoacetanilide STEP 1: Hydrochloric Acid + Sodium Chlorate --> Chlorine + Water + Sodium Chloride STEP 2: 4-Bromoacetanilide + Chlorine --> 4-Bromo-2-Chloroacetanilide 4-Bromo-2-Chloroacetanilide + Ethanol --> 4-Bromo-2-Chloroaniline + Ethyl Acetate Show all lone pairs or formal charges.
Draw the structure of p-bromophenol and 2-bromo-4-iodotoluene. Name the following:
1) a) Draw 2-bromo-3-phenylpentanal. b) Draw 4-ethyl-6-methyl-3-heptanone.
Draw all stereoisomers of 4-bromo-2-pentene. Position the groups attached to the double bond (120° bond angles) to indicate its stereochemistry. Don't use bold wedges,hashed wedges, or wavy or criss-cross bonds to indicate double-bond stereochemistry. Do use bold and hashed wedges to indicate the configuration at C(sp3)stereocenters.*please help!!