2. Provide the reagents needed to accomplish the following transformations. If more than one step is needed per transformation, be sure to number them appropriately. Stron remove Kol-l 1.HCH2, mg Br 2 HsO 3. HBra TSCl H2/Pd 2. H3ot Br Strong bases are nore likely to lepronatélrerouing) the hydrogen +then Kickoff Br. .Toreduce ce use a grinad and the ethy will attach (C and 3.(HBr). add Br. 3. T5cl, PY 4 HaBu OK step 3.0 This ste is veducing

||| O ORGANIC FUNCTIONAL GROUPS Predicting the products of symmetric alcohol dehydration Predict the missing product of this organic reaction: H+ A OH planation + H₂O Specifically, in the drawing area below draw the skeletal ("line") structure of P. Click and drag to start drawing a structure. Check www-awu.alek

Please answer very soon

1-6.) Match the following formulae with their representative organic compounds. 4) C12H22011 D) lactone 1) C6H120 A) aldehyde 2) C6H14O3 B) keto acid 3) CH10O2 C) triol 5) СHs E) lactose 6) C12H2203 F) cyclic diene

What is the name of this molecule? (look at the picture to be able to answer) a) 4-bromo-6-ethylcyclohex-1-ene b) 4-bromo-6-ethylcyclobenzene c) 1-bromo-3-ethylbenzene d) 3-bromotoluene m-bromotoluene e) 5-bromo-3-ethylcyclohexene f) Nothing is correct.

Can someone explain why I got this question wrong?

Which name is correct for the following 3 dots molecule? OH nonane CI a) 6-chloro-7-ethyl-3-decanol b) 4-chloro-7-hydroxy-3-propyl- c) 6-chloro-3-hydroxy-7-propyl- nonanol d) 5-chloro-4-ethyl-8-decanol e) 6-chloro-7-propyl-3-nonanol

Highlight in red each acidic location on the organic molecule at left. Highlight in blue each basic location on the organic molecule at right. Note for advanced students: we mean acidic or basic in the Brønsted-Lowry sense only. N Cl N CI X

A Moving to another question will save this response. Question 2 Which of the following compounds has the IUPAC name hexane? O CH3(CH2)4CH3 O CH3CH2CH2CH3 O CH3CH3 O CH3(CH2)3CH3 AMoving to another question will save this response. F2