Can someone explain to me why OH is ranked second and Ch3Ch2 is ranked 3rd?
Can someone explain to me why OH is ranked second and Ch3Ch2 is ranked 3rd? CH₂...
can someone show me how to do the work and explain it to me
10. What is the leaving group in the following reaction? CH,CHOH + HCI , CHCHCI + 0 А. ОН НО CH3CH, CI D.
Can someone explain why they are ranked in this particular
order? Thank you.
6) (3 pts) Rank the following in order of increasing reactivity via Sp2 (lowest = 1, highest = 3)
Please can someone help me with this? I can not figure out
which molecules match up with the terms in A) and B)
James Howland CHEM 1121: General, Organic, & Biochemistry Identifying Biomolecules A) Label each of the molecules shown according to which type it is: carbohydrate lipid fatty acid water-soluble vitamin B) with one exception, all of the molecules shown are also one of these sub-types. Label the molecules with the appropriate sub-types. disaccharide fat-soluble vitamin monosaccharide phospholipid saturated...
can
you show me the IUPAC NAMES
- Lower Z configuration Higher ranked substituents (Cl and Br) are on same side of double bond Lower - H B r Higher E configuration Higher ranked substituents (Cl and Br) are on opposite sides of double bond Problem 7.7 Determine the configuration of each of the following as Zor E as appropriate: Y OH Sample Solution (a) One of the doubly bonded carbons bears a methyl group and a Page 251 hydrogen....
why is the answer D and not A? can someone draw this out and
explain for me? i thought the K2CrO7 would not affect the Br? thank
you so much!
71. Which set of reagents would synthesize m-bromobenzoic acid from benzene? um benzene? F E D a) CH3CI, AICI3; Br2 FeBrz: K2Cr 07, H30 b) CHCI, AICI: Br, FeBrz: KMnO4, H20 c) Br, FeBrz; CH CI, AICI3; K,Cr,0. Hz0 d) CHZCI, AICI:: K Cro, H20 : Bry, FeBrz e) Br,...
someone finish the first reaction snd check my second
one?
Scheme 1: C3H₂O C4 H2O2 Br Compound 2 Compound 1 12504 /194 11.94 1.14 H (b) OH (a) OH он Etot Br Compound 4 Sympound 3 (c) OH Scheme 2: Compound 5 Compound 6 Compound 2 (d) (e) ° 7 CHIO O Co Hiyo C&H 13 CI 디 OH HEL i CH₂ Mg Br На 09
CAN SOMEONE PLEASE ANSWER THESE FOR ME QUICKLY!!!
Name: O Determine wither a reaction proceeds via SN2, SN1, E2, and/or E1/ Predict the productís) of substitution and elimination reactions. Draw the major products), reagent(s), or starting material(s) ¡n order to complete each transformation. Indicate any stereochemistry when appropriate. If there is no reaction, write "NO RXN AND explain why no reaction occurs 1. Br NaCCMe Br b. он NaOE Me DBU d. MeOH e. CI NaSEt Chapter 8-3
Can someone please help me with these and quick!!! its okay to
not do all of them, but please help!
26.) 3 points each) Draw the organic product which results from each of the following reaction conditions. KM04 HÀ GHI a.) E10 b.) Вон NON coa d.) Men CH- 1. LIAR 2.0" och ACES f) BY2 Feb NOR 8.) I SOCI 1 CH ( 4 0. h.) ..) 1, CH MÊ .CN j.) 2. H2O k.) no 2. CO 3....
Hi can someone explain why this is a diastermer I’m not able
to figure out the configuration of the ch3 because isn’t that
achril because of the two oh groups ? Can someone show if it is the
chiral the priority groups labeled around the ch3 ?
For the second picture is this answer key wrong because I’m
getting a solid wedge for ethyl not dashed ??
all-cis all-trans CH3 CH3 но но diastereomer он он
Correct answers are #4 and #1. But can someone help me
understand why???
14. What is the product of the reaction below? NaCN (1 equiv) Ω NC 1) 2) ON 3) NC 8. 4) "CN 5) 15. Which would be the best reaction to synthesize the product below? SCH CI NaSCHE NaSCHE 1) 2) Br NaSCH 3)